What is the (±)-Kaura-16-ene?

(±)-Kaura-16-ene is , while it's Molecular Formula is C20H32. Used in Pharmaceutical Industry: (±)-Kaura-16-ene is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique chemical structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways. Used in Chemical Synthesis: (±)-Kaura-16-ene serves as a valuable building block in the synthesis of complex organic molecules. Its tetracyclic diterpene structure makes it a versatile starting material for creating a wide range of chemical compounds, including natural products and bioactive molecules. Used in Research and Development: (±)-Kaura-16-ene is utilized as a research tool in the study of diterpene biosynthesis, structure-activity relationships, and the development of novel chemical reactions. Its unique properties make it an interesting subject for scientific investigation and potential applications in various fields. Used in Agrochemical Industry: (±)-Kaura-16-ene may be employed as a component in the development of agrochemicals, such as pesticides and herbicides. Its chemical structure could be exploited to target specific pests or weeds, providing an effective and environmentally friendly solution for agricultural challenges. Used in Flavor and Fragrance Industry: Due to its unique chemical structure, (±)-Kaura-16-ene could be used as a component in the creation of new flavors and fragrances. Its potential to contribute to the development of novel scents and tastes makes it an interesting candidate for the flavor and fragrance industry.

What is the CAS number for (±)-Kaura-16-ene?

The CAS number of (±)-Kaura-16-ene is 562-28-7.

What is (±)-Kaura-16-ene (562-28-7) used for?

(±)-Kaura-16-ene is a tetracyclic diterpene derived from the ent-kaurane family, characterized by the replacement of the 6-methyl group with a methylene group. This organic compound is known for its unique chemical structure and potential applications in various industries.InChI:InChI=1/C20H32/c1-14-12-20-11-8-16-18(2,3)9-5-10-19(16,4)17(20)7-6-15(14)13-20/h15-17H,1,5-13H2,2-4H3/t15-,16-,17+,19-,20-/m0/s1

What is the (±)-Kaura-16-ene?

(±)-Kaura-16-ene is , while it's Molecular Formula is C20H32. Used in Pharmaceutical Industry: (±)-Kaura-16-ene is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique chemical structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways. Used in Chemical Synthesis: (±)-Kaura-16-ene serves as a valuable building block in the synthesis of complex organic molecules. Its tetracyclic diterpene structure makes it a versatile starting material for creating a wide range of chemical compounds, including natural products and bioactive molecules. Used in Research and Development: (±)-Kaura-16-ene is utilized as a research tool in the study of diterpene biosynthesis, structure-activity relationships, and the development of novel chemical reactions. Its unique properties make it an interesting subject for scientific investigation and potential applications in various fields. Used in Agrochemical Industry: (±)-Kaura-16-ene may be employed as a component in the development of agrochemicals, such as pesticides and herbicides. Its chemical structure could be exploited to target specific pests or weeds, providing an effective and environmentally friendly solution for agricultural challenges. Used in Flavor and Fragrance Industry: Due to its unique chemical structure, (±)-Kaura-16-ene could be used as a component in the creation of new flavors and fragrances. Its potential to contribute to the development of novel scents and tastes makes it an interesting candidate for the flavor and fragrance industry.

What is the CAS number for (±)-Kaura-16-ene?

The CAS number of (±)-Kaura-16-ene is 562-28-7.

What is (±)-Kaura-16-ene (562-28-7) used for?

(±)-Kaura-16-ene is a tetracyclic diterpene derived from the ent-kaurane family, characterized by the replacement of the 6-methyl group with a methylene group. This organic compound is known for its unique chemical structure and potential applications in various industries.InChI:InChI=1/C20H32/c1-14-12-20-11-8-16-18(2,3)9-5-10-19(16,4)17(20)7-6-15(14)13-20/h15-17H,1,5-13H2,2-4H3/t15-,16-,17+,19-,20-/m0/s1

Product classification

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562-28-7

Product Name:ent-kaurane
Molecular Formula:C20H32
Molecular Weight:272.474

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Product Details

pd_meltingpoint:51 °C

Purity:99%

Factory Sells Best Quality ent-kaurane 562-28-7 with ISO standards

Molecular Formula:C20H32
Molecular Weight:272.474
Vapor Pressure:0.000111mmHg at 25°C
Melting Point:51 °C
Boiling Point:346.9°C at 760 mmHg
Flash Point:170.3°C
PSA：0.00000
Density:0.97g/cm³
LogP:5.97540

(±)-Kaura-16-ene(Cas 562-28-7) Usage

Definition

ChEBI: A tetracyclic diterpene consisting of ent-kaurane, where the 6-methyl group is replaced by methylene.

InChI:InChI=1/C20H32/c1-14-12-20-11-8-16-18(2,3)9-5-10-19(16,4)17(20)7-6-15(14)13-20/h15-17H,1,5-13H2,2-4H3/t15-,16-,17+,19-,20-/m0/s1

562-28-7 Relevant articles

Functional characterization of wheat ent-kaurene(-like) synthases indicates continuing evolution of labdane-related diterpenoid metabolism in the cereals

Zhou, Ke,Xu, Meimei,Tiernan, Mollie,Xie, Qian,Peters, Reuben J.,Toyomasu, Tomonobu,Sugawara, Chizu,Oku, Madoka,Usui, Masami,Mitsuhashi, Wataru,Chono, Makiko,Chandler, Peter M.

, p. 47 - 55,9 (2012/12/12)

Wheat (Triticum aestivum) and rice (Oryz...

Functional characterization of wheat ent-kaurene(-like) synthases indicates continuing evolution of labdane-related diterpenoid metabolism in the cereals

Zhou, Ke,Xu, Meimei,Tiernan, Mollie,Xie, Qian,Toyomasu, Tomonobu,Sugawara, Chizu,Oku, Madoka,Usui, Masami,Mitsuhashi, Wataru,Chono, Makiko,Chandler, Peter M.,Peters, Reuben J.

, p. 47 - 55 (2013/01/15)

Wheat (Triticum aestivum) and rice (Oryz...

Synthesis of ent-Kaurene from a Naturally Occurring Precursor

Hogg, Ronald W.,Knox, John R.

, p. 469 - 474 (2007/10/02)

ent-Kaurene (1) has been synthesized fro...

Synthesis and Evaluation of Cyclobutylcarbinyl Derivatives as Potential Intermediates in Diterpene Biosynthesis

Coates, Robert M.,Kang, Han-Young

, p. 2065 - 2074 (2007/10/02)

A new mechanism for the enzyme-catalyzed...

562-28-7 Process route

: 150-97-0,690-72-2,17817-88-8,32451-23-3
D,L-mevalonic acid

: 469-85-2,469-86-3,562-28-7,10178-84-4,13850-19-6,20070-61-5,87759-99-7
kaurene

: 1164-45-0
gibberellin A₁₂

: 5095-09-0,6730-83-2,14046-76-5,19941-50-5,20316-84-1,34426-48-7,98523-71-8
kaurenoic acid

: 77280-78-5
ent-kaura-6,16-dien-19-oic acid

Conditions

Conditions	Yield
With cell-free system of Phaseolus coccineus; K-Pi buffer; NADPH; bovine serum albumin; at 28 - 30 ℃; for 2h; Further byproducts given;

: 112609-07-1
ent-17-iodokaurane

: 469-85-2,469-86-3,562-28-7,10178-84-4,13850-19-6,20070-61-5,87759-99-7
kaurene

Conditions

Conditions	Yield
With potassium tert-butylate; In dimethyl sulfoxide; at 78 ℃; for 2h;	2.9 g

562-28-7 Upstream products

36146-33-5
ent-15-Kauren-6-on-20-al
112609-07-1
ent-17-iodokaurane
90457-97-9
ent-kauran-17-ol
28235-66-7
ent-15-Kauren-6α,20-diol

562-28-7 Downstream products

10179-10-9
(-)-Kauren-(16)-ol-(15α)
10438-44-5
(-)-kaur-16-en-19-ol
5282-24-6
ent-kaur-16-en-19-al
5095-09-0
kaurenoic acid

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