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Benzeneacetic acid, a-methyl-4-(2-methylpropyl)-, lithium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183664-35-9

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183664-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183664-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,6,6 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 183664-35:
(8*1)+(7*8)+(6*3)+(5*6)+(4*6)+(3*4)+(2*3)+(1*5)=159
159 % 10 = 9
So 183664-35-9 is a valid CAS Registry Number.

183664-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Lithium Salt of Ibuprofen

1.2 Other means of identification

Product number -
Other names -

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:183664-35-9 SDS

183664-35-9Upstream product

183664-35-9Downstream Products

183664-35-9Relevant academic research and scientific papers

Enantiomeric resolution of aryl-substituted aliphatic carboxylic acids

-

, (2008/06/13)

A process for obtaining a substantially pure enantiomer of an aryl-substituted aliphatic carboxylic acid is described. The process utilizes first an enantiomerically enriched mixture the of aryl-substituted aliphatic carboxylic acid obtained from kinetic resolution, diastereomeric crystallization or asymmetric synthesis processes. This enriched mixture is reacted with a base producing a salt that has the following properties: 1) has at least one eutectic point; 2) a composition that is not at the eutectic point; and 3) a eutectic composition that is closer to the racemic composition than is the eutectic composition of said aryl-substituted carboxylic acid. Substantially pure, enantiomeric salt is separated, leaving a mother liquor comprising the solvent and aryl-substituted aliphatic carboxylic acid enriched in the other enantiomer.

Enantiomeric resolution

-

, (2008/06/13)

A process for obtaining a substantially pure enantiomer of an aryl-substituted aliphatic carboxylic acid is described. The process utilizes first an enantiomerically enriched mixture the of aryl-substituted aliphatic carboxylic acid obtained from kinetic resolution, diastereomeric crystallization or asymmetric synthesis processes. This enriched mixture is reacted with a base producing a salt that has the following properties: (1) has at least one eutectic point; (2) a composition that is not at the eutectic point; and (3) a eutectic composition that is closer to the racemic composition than is the eutectic composition of said aryl-substituted carboxylic acid. Substantially pure, enantiomeric salt is separated, leaving a mother liquor comprising the solvent and aryl-substituted aliphatic carboxylic acid enriched in the other enantiomer.

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