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3,3,3-trichlorolactic acid is a synthetic organic compound with the chemical formula C3H2Cl3O3. It is a halogenated derivative of lactic acid, where three hydrogen atoms are replaced by chlorine atoms. 3,3,3-trichlorolactic acid is known for its potential use as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its reactivity and the presence of multiple chlorine atoms, it can be involved in a range of chemical reactions, making it a versatile building block in organic chemistry. However, it is important to handle such halogenated compounds with care due to their potential environmental and health impacts.

599-01-9

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599-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 599-01-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 599-01:
(5*5)+(4*9)+(3*9)+(2*0)+(1*1)=89
89 % 10 = 9
So 599-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H3Cl3O3/c4-3(5,6)1(7)2(8)9/h1,7H,(H,8,9)

599-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,3-trichloro-2-hydroxypropanoic acid

1.2 Other means of identification

Product number -
Other names EINECS 209-962-8

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:599-01-9 SDS

599-01-9Relevant academic research and scientific papers

Synthesis of F-alkyl α-hydroxy acids and esters from F-alkyl epoxides and F-alkyl α-bromo acids and esters from F-alkyl bromohydrins

Ould Amanetoullah,Chaabouni,Baklouti

, p. 149 - 153 (2007/10/03)

F-alkyl α-hydroxy acids and F-alkyl α-bromo acids were prepared respectively by the nitric acid ring-opening oxidative reaction of F-alkyl oxiranes, and oxidation by chromic acid of F-alkyl bromohydrins. The synthesized acids were converted to the corresponding methyl esters which may prove to be useful in the synthesis of F-alkylated heterocycles.

Carbonylation of trichloroacetaldehyde (chloral) in concentrated sulfuric acid: Stereocontrolled synthesis of cis- and trans-2,5-bis(trichloromethyl)-1,3-dioxolan-4-one

Mori, Sadayuki,Emura, Kazuhiro,Kano, Motoaki,Kudo, Kiyoshi,Komatsu, Koichi,Sugita, Nobuyuki

, p. 8977 - 8982 (2007/10/02)

Carbonylation of trichloroacetaldehyde(chiral) in concentrated sulfuric acid readily gave 2,5-bis(trichloromethyl-1,3-dioxolan-4-ones (cis and trans) and 3,3,3-trichloro-2-hydroxypropanoic acid. The cis isomer was isolated for the first time, and confirmed by X-ray structural analysis. The cis/trans ratio of dioxolanones largely depended upon the concentration of sulfuric acid. Highly diastereoselective formation of the dioxolanones was achieved with 99wt% sulfuric acid (cis:trans = 95:5) or with 90wt% sulfuric acid (0:100).

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