What is the (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid?

(2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is , while it's Molecular Formula is C 10 H 12 O 3 . Used in Pharmaceutical Industry: (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is used as a precursor for the synthesis of various drugs due to its unique chemical structure and potential biological activities. Used in Flavor and Fragrance Industry: (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is used as a building block for the production of flavors and fragrances, taking advantage of its natural occurrence and unique chemical properties. Used in Research and Development: (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is used in research and development for studying its potential biological activities, such as anti-inflammatory and anti-cancer properties, and exploring its applications in various fields.

What is the CAS number for (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid?

The CAS number of (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is 76549-02-5.

What is the (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid?

(2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is , while it's Molecular Formula is C 10 H 12 O 3 . Used in Pharmaceutical Industry: (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is used as a precursor for the synthesis of various drugs due to its unique chemical structure and potential biological activities. Used in Flavor and Fragrance Industry: (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is used as a building block for the production of flavors and fragrances, taking advantage of its natural occurrence and unique chemical properties. Used in Research and Development: (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is used in research and development for studying its potential biological activities, such as anti-inflammatory and anti-cancer properties, and exploring its applications in various fields.

What is the CAS number for (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid?

The CAS number of (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is 76549-02-5.

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76549-02-5

Q: What is (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid (76549-02-5) used for?

(2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is a chiral molecule with a molecular formula C10H12O3. It is a derivative of phenylpropanoic acid and is commonly found in natural products such as plants and fungi. (2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid has two stereoisomers, which are mirror images of each other, and has been studied for its potential biological activities, including anti-inflammatory and anti-cancer properties.

Product Name:3-Hydroxy-2-methyl-3-phenylpropanoic acid
Molecular Weight:180.203

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Product Details

Purity:99%

High Quality Chinese Factory supply 76549-02-5 3-Hydroxy-2-methyl-3-phenylpropanoic acid

Molecular Formula:C₁₀H₁₂O₃
Molecular Weight:180.203

76549-02-5 Relevant articles

Synthesis and Enantioselective Aldol Reaction of a Chiral 2-Oxo-2-propionyl-1,3,2-oxazaphosphorinane

Gordon, Neil J.,Evans, Slayton A.

, p. 5295 - 5297 (1993)

The synthesis of cis- and trans-2-oxo-2-...

Synthesis and evaluation of a new non-cross-linked polystyrene supported hydantoin chiral auxiliary for asymmetric aldol reactions

Lu, Guang-Jun,Nie, Jun-Qi,Chen, Zu-Xing,Yang, Gui-Chun,Lu, Cui-Fen

, p. 1331 - 1335 (2013)

A new non-cross-linked polystyrene suppo...

Siloxy Esters as Traceless Activators of Carboxylic Acids: Boron-Catalyzed Chemoselective Asymmetric Aldol Reaction**

Fujita, Taiki,Kanai, Motomu,Mitsunuma, Harunobu,Sameera, W. M. C.,Yamane, Mina

supporting information, p. 24598 - 24604 (2021/10/14)

The catalytic asymmetric aldol reaction ...

Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged chiral oxazolidinones

Turkyilmaz, Serhan,Wilcox, Craig S.

supporting information, p. 2031 - 2033 (2017/05/04)

Sorting tags are oligomeric structures t...

Anti-Selective enolboration-aldolization of propanoic acid

Ramachandran, P. Veeraraghavan,Chanda, Prem B.,Otoo, Barnabas

supporting information, p. 1289 - 1291 (2014/03/21)

A systematic examination of enolboration...

Enantio- and diastereoselective hetero-Diels-Alder reactions between 4-methyl-substituted Rawal's diene and aldehydes catalyzed by chiral dirhodium(II) carboxamidates: Catalytic asymmetric synthesis of (-)-cis-aerangis lactone

Watanabe, Yudai,Shimada, Naoyuki,Anada, Masahiro,Hashimoto, Shunichi

, p. 63 - 73 (2014/02/14)

The first catalytic asymmetric hetero-Di...

76549-02-5 Process route

: 65946-51-2
2-(Trimethylsilyl)propansaeure-trimethylsilylester

: 100-52-7
benzaldehyde

: 13545-04-5
2,3-dimethylsuccinic acid

: 14366-86-0,14366-87-1,23985-58-2,36041-79-9,64869-25-6,68040-42-6,76549-02-5,76549-04-7,116126-02-4
(2RS, 3SR)-3-hydroxy-2-methyl-3-phenylpropanoic acid

: 64869-25-6
syn-3-hydroxy-2-methyl-3-phenylpropanoic acid

Conditions

Conditions	Yield
Product distribution; other catalysts discussed;

: (S)-3-((2S,3S)-3-hydroxy-2-methyl-3-phenylpropionyl)-4-[4-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)benzyl]oxazolidin-2-one

: 76549-02-5
(-)-(2S,3S)-3-hydroxy-2-methyl-3-phenylpropanoic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; lithium hydroxide; In tetrahydrofuran; water; at 0 - 20 ℃; for 2h;	91%

76549-02-5 Upstream products

77877-25-9
(4S)-3-((2S,3S)-3-hydroxy-2-methyl-1-oxo-3-phenylpropyl)-4-(1-methylethyl)-2-oxazolidinone
131701-06-9
(2S,3S)-3-Hydroxy-2-methyl-1-((R)-3-methyl-1,1-dioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-3-phenyl-propan-1-one
132939-79-8
(1S,2S,4S)-1,4-dihydroxy-2,5,5-trimethyl-1-phenyl-3-hexanone
76549-03-6
methyl (2S,3S)-3-hydroxy-2-methyl-3-phenylpropanoate

76549-02-5 Downstream products

76549-03-6
methyl (2S,3S)-3-hydroxy-2-methyl-3-phenylpropanoate
16251-45-9
(4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one
101450-38-8
(2RS,3SR)-3-hydroxy-2-methyl-3-phenyl-propionic acid-(2-diethylamino-ethyl ester)
116126-02-4
(+)-(2S,3R)-3-hydroxy-2-methyl-3-phenylpropanoic acid

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