What is the 1-(1,3-benzodioxol-5-yl)propan-2-ol?

1-(1,3-benzodioxol-5-yl)propan-2-ol is , while it's Molecular Formula is C10H12O3. Used in Fragrance Industry: 1-(1,3-benzodioxol-5-yl)propan-2-ol is used as a key ingredient in the fragrance industry for its sweet, floral scent, contributing to the creation of various perfumes and scented products. Used in Flavorings Industry: In the flavorings industry, safrole alcohol is utilized for its distinctive aroma to enhance the taste of food products and beverages. Used in Pharmaceutical Industry: Safrole alcohol serves as a precursor in the synthesis of certain pharmaceuticals, although its use in this context is carefully controlled due to its toxicological profile. Used as a Precursor in Synthesis: 1-(1,3-benzodioxol-5-yl)propan-2-ol is used as a chemical precursor in the synthesis of recreational drugs like MDMA (ecstasy), but this application is illicit and heavily regulated due to the compound's potential for abuse and health risks.

What is the CAS number for 1-(1,3-benzodioxol-5-yl)propan-2-ol?

The CAS number of 1-(1,3-benzodioxol-5-yl)propan-2-ol is 6974-61-4.

What is 1-(1,3-benzodioxol-5-yl)propan-2-ol (6974-61-4) used for?

1-(1,3-benzodioxol-5-yl)propan-2-ol, also known as 1-(3,4-methylenedioxyphenyl)-2-propanol, is a chemical compound with the molecular formula C10H12O3. It is a colorless liquid with a molecular weight of 180.20 g/mol. 1-(1,3-benzodioxol-5-yl)propan-2-ol is a derivative of propanol, featuring a 1,3-benzodioxole (also known as methylene dioxy) group attached to the propanol backbone. The benzodioxole ring consists of a benzene ring with two oxygen atoms connected to adjacent carbon atoms, creating a methylene bridge. This structure is significant in the synthesis of various pharmaceuticals and natural products, as it can be found in compounds with potential therapeutic properties. The compound is also known for its role in the synthesis of certain psychoactive substances, although it is not itself psychoactive. It is important to note that the handling and use of such chemicals should be done with proper safety measures and in accordance with relevant regulations.

What is the 1-(1,3-benzodioxol-5-yl)propan-2-ol?

1-(1,3-benzodioxol-5-yl)propan-2-ol is , while it's Molecular Formula is C10H12O3. Used in Fragrance Industry: 1-(1,3-benzodioxol-5-yl)propan-2-ol is used as a key ingredient in the fragrance industry for its sweet, floral scent, contributing to the creation of various perfumes and scented products. Used in Flavorings Industry: In the flavorings industry, safrole alcohol is utilized for its distinctive aroma to enhance the taste of food products and beverages. Used in Pharmaceutical Industry: Safrole alcohol serves as a precursor in the synthesis of certain pharmaceuticals, although its use in this context is carefully controlled due to its toxicological profile. Used as a Precursor in Synthesis: 1-(1,3-benzodioxol-5-yl)propan-2-ol is used as a chemical precursor in the synthesis of recreational drugs like MDMA (ecstasy), but this application is illicit and heavily regulated due to the compound's potential for abuse and health risks.

What is the CAS number for 1-(1,3-benzodioxol-5-yl)propan-2-ol?

The CAS number of 1-(1,3-benzodioxol-5-yl)propan-2-ol is 6974-61-4.

What is 1-(1,3-benzodioxol-5-yl)propan-2-ol (6974-61-4) used for?

1-(1,3-benzodioxol-5-yl)propan-2-ol, also known as 1-(3,4-methylenedioxyphenyl)-2-propanol, is a chemical compound with the molecular formula C10H12O3. It is a colorless liquid with a molecular weight of 180.20 g/mol. 1-(1,3-benzodioxol-5-yl)propan-2-ol is a derivative of propanol, featuring a 1,3-benzodioxole (also known as methylene dioxy) group attached to the propanol backbone. The benzodioxole ring consists of a benzene ring with two oxygen atoms connected to adjacent carbon atoms, creating a methylene bridge. This structure is significant in the synthesis of various pharmaceuticals and natural products, as it can be found in compounds with potential therapeutic properties. The compound is also known for its role in the synthesis of certain psychoactive substances, although it is not itself psychoactive. It is important to note that the handling and use of such chemicals should be done with proper safety measures and in accordance with relevant regulations.

Product classification

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6974-61-4

Product Name:1-(1,3-benzodioxol-5-yl)propan-2-ol
Molecular Formula:C₁₀H₁₂O₃
Molecular Weight:180.203

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Product Details

Purity:99%

Buy cost-effective 99% pure 1-(1,3-benzodioxol-5-yl)propan-2-ol 6974-61-4 now

Molecular Formula:C10H12O3
Molecular Weight:180.203
Vapor Pressure:0.000856mmHg at 25°C
Boiling Point:292.1°Cat760mmHg
Flash Point:130.5°C
Density:1.219g/cm³

6974-61-4 Relevant articles

Markovnikov Wacker-Tsuji Oxidation of Allyl(hetero)arenes and Application in a One-Pot Photo-Metal-Biocatalytic Approach to Enantioenriched Amines and Alcohols

Albarrán-Velo, Jesús,Gotor-Fernández, Vicente,Lavandera, Iván

, p. 4096 - 4108 (2021/08/19)

The Wacker-Tsuji aerobic oxidation of va...

Chemoenzymatic synthesis of enantiomerically pure syn-configured 1-aryl-3-methylisochroman derivatives

Simon, Robert C.,Busto, Eduardo,Richter, Nina,Belaj, Ferdinand,Kroutil, Wolfgang

, p. 111 - 121 (2014/01/06)

A two-step synthesis of various enantiom...

A simple and efficient synthesis of GYKI 52466 and GYKI 52895

Zappala, Maria,Grasso, Silvana,Micale, Nicola,Polimeni, Santina,De Micheli, Carlo

, p. 527 - 533 (2007/10/03)

The synthesis of 1-(4-aminophenyl)-4-met...

Sodium Perborate: A Mild and Convenient Reagent for Efficiently Oxidizing Organoboranes

Kabalka, George W.,Shoup, Timothy M.,Goudgaon, Naganna M.

, p. 5930 - 5933 (2007/10/02)

Sodium perborate, a readily available an...

6974-61-4 Process route

: 7470-44-2
safrole 2',3'-oxide

: 6974-61-4
β-oxy-α-(3',4'-methylenedioxyphenyl)propane

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal; In methanol; for 3h; under 3361.5 Torr;	90%

: 94-59-7
1-allyl-3,4-methylenedioxybenzene

: 6974-61-4
β-oxy-α-(3',4'-methylenedioxyphenyl)propane

Conditions

Conditions	Yield
1-allyl-3,4-methylenedioxybenzene; With mercury(II) diacetate; In tetrahydrofuran; at 20 ℃; for 1h; With sodium hydroxide; sodium tetrahydroborate; In tetrahydrofuran; for 1h;	96%
With sodium hydroxide; sodium tetrahydroborate; mercury(II) diacetate; Yield given. Multistep reaction; 1.) THF/H₂O, room temp., 1 h; 2.) THF/H₂O, 1 h;
Multi-step reaction with 2 steps 1: 80 percent / CH₃CO₃H / CHCl₃ / 72 h / Ambient temperature 2: 90 percent / H₂ / 10percent Pd/C / methanol / 3 h / 3361.5 Torr With peracetic acid; hydrogen; palladium on activated charcoal; In methanol; chloroform;
Multi-step reaction with 2 steps 1: dichloro bis(acetonitrile) palladium(II); 9-(2-mesityl)-10-methylacridinium perchlorate / acetonitrile / 16 h / 20 °C 2: sodium tetrahydroborate / methanol With dichloro bis(acetonitrile) palladium(II); sodium tetrahydroborate; 9-(2-mesityl)-10-methylacridinium perchlorate; In methanol; acetonitrile; 1: \|Wacker-Tsuji Olefin Oxidation;

6974-61-4 Upstream products

94-59-7
1-allyl-3,4-methylenedioxybenzene
4676-39-5
1-(1,3-benzodioxol-5-yl)-2-propanone
7470-44-2
safrole 2',3'-oxide
120-57-0
piperonal

6974-61-4 Downstream products

4676-39-5
1-(1,3-benzodioxol-5-yl)-2-propanone
379733-75-2
trans-7,8-dihydro-7-methyl-5-(4-nitrophenyl)-5H-[1,3]dioxolo[4,5-g][2]benzopyrane
172542-26-6
(S)-α-methyl-1,3-benzodioxole-5-ethanol
521097-97-2
(R)-1-[3,4-(methylenedioxy)phenyl]propan-2-ol

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