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108365-31-7

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108365-31-7 Usage

Uses

water soluble store desiccated at –20°C

Check Digit Verification of cas no

The CAS Registry Mumber 108365-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,6 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108365-31:
(8*1)+(7*0)+(6*8)+(5*3)+(4*6)+(3*5)+(2*3)+(1*1)=117
117 % 10 = 7
So 108365-31-7 is a valid CAS Registry Number.

108365-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name KAINIC ACID DIMETHYL ESTER HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names ((3S)-4c-Isopropenyl-2t-methoxycarbonyl-pyrrolidin-3r-yl)-essigsaeure-methylester,Hydrochlorid

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:108365-31-7 SDS

108365-31-7Downstream Products

108365-31-7Relevant articles and documents

Parallel synthesis of novel heteroaromatic acromelic acid analogues from kainic acid

Baldwin,Fryer,Pritchardt

, p. 2588 - 2596 (2007/10/03)

A range of new C-4 heteroaromatic acromelic acid analogues has been synthesized in a parallel fashion from (-)-α-kainic acid 1. Protection of the amine and carboxylate groups of 1 followed by ozonolysis gave methyl ketone 8. A silyl enol ether 9, generated regiospecifically from the methyl ketone 8 using "kinetic" conditions, was brominated in situ with phenyltrimethylammonium perbromide to give the key α-bromo ketone 10. Parallel cyclization reactions of bromo ketone 10 with thioamides and thioureas were then performed. The aromatic heterocyclic derivatives 11a-d and 19 produced were deprotected to give the new kainoid amino acids 6a-d and 25 in excellent yield. Compounds 6a and 6c show strong binding to the kainate receptor. Reaction of 10 with alternative condensing agents was also briefly investigated.

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