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Benzenepropanoic acid, 3-chloro-β-hydroxy-, also known as 3-chloro-β-hydroxybenzenepropanoic acid, is an organic compound with the chemical formula C9H9ClO3. It is a derivative of benzenepropanoic acid, featuring a chlorine atom at the 3rd carbon position and a hydroxyl group at the β-carbon. Benzenepropanoic acid, 3-chloro-b-hydroxy- is a white crystalline solid and is soluble in water, ethanol, and other organic solvents. It has various applications in the pharmaceutical and chemical industries, such as a building block for the synthesis of drugs and other organic compounds. Due to its chemical structure, it exhibits properties like acidity and reactivity towards nucleophiles, making it a versatile intermediate in organic synthesis.

40620-64-2

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40620-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40620-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,2 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40620-64:
(7*4)+(6*0)+(5*6)+(4*2)+(3*0)+(2*6)+(1*4)=82
82 % 10 = 2
So 40620-64-2 is a valid CAS Registry Number.

40620-64-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-3-(3'-chlorophenyl)propionic acid

1.2 Other means of identification

Product number -
Other names (S)-3-(3'-chlorophenyl)-3-hydroxypropanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:40620-64-2 SDS

40620-64-2Relevant academic research and scientific papers

NOVEL 2'-C-METHYL AND 4'-C-METHYL NUCLEOSIDE DERIVATIVES

-

Page/Page column 107-108, (2008/06/13)

Novel 2'-C-methyl nucleoside 5 '-monophosphate and 4'-C-methyl nucleoside 5'- monophosphate derivatives, stereoisomers, and pharmaceutically acceptable salts or prodrugs thereof, their preparation, and their uses for the treatment of hepatitis C viral inf

Structures of Racemic Halogen-Substituted 3-Hydroxy-3-phenylpropionic Acids; Relations Between Spontaneously Resolved and Racemic Compounds

Larsen, Sine,Marthi, Katalin

, p. 338 - 346 (2007/10/02)

Low-temperature X-ray diffraction data showed that racemic 3-hydroxy-3-(3'-chlorophenyl)propionic acid and its bromo-substituted analogue are isostructural. 3-Hydroxy-3-(3'-chlorophenyl)propionic acid: C9H9ClO3, Mr = 200.61, monoclinic, P21/c, a = 15.301 (2), b = 5.7117 (8), c = 11.2462 (13) Angstroem, β = 110.873 (10) deg, V = 918.4 (2) Angstroem3, Z = 4, Dx = 1.451 g cm-3, μ = 35.15 cm-1, F(000) = 416, wR2 = 0.0775 for 1880 contributing reflections 4?(F)>, m.p. 342.7(5) K. 3-Hydroxy-3-(3'-bromophenyl)propionic acid: C9H9BrO3, Mr = 245.07, monoclinic, P21/c, a = 15.498 (3), b = 5.7513 (12), c = 11.298 (2) Angstroem, β = 111.280 (14) deg, V = 938.4 (3) Angstroem3, Z = 4, Dx = 1.735 g cm-3, μ = 58.07 cm-1, F(000) = 488, wR2 = 0.0769 for 1926 contributing reflections 4?(F)>, m.p. 348.7(5) K.The results from these structure determinations were combined with results from crystal structure determinations of other halogen-substituted 3-hydroxy-3-phenylpropionic acids in an analysis performed to obtain insight into their conglomerate versus racemic compound formation.In all the structures studied, the O-H...O hydrogen bonds are formed between identical donor and acceptor atoms leading to two distinct motifs.The crystallization of the racemates as either racemic compounds or mechanical mixtures of enantiomers can only be rationalized if weaker intermolecular interactions are taken into account.

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