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123941-02-6

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123941-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123941-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123941-02:
(8*1)+(7*2)+(6*3)+(5*9)+(4*4)+(3*1)+(2*0)+(1*2)=106
106 % 10 = 6
So 123941-02-6 is a valid CAS Registry Number.

123941-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[2-(2,6-dimethylanilino)-2-oxoethyl]amino]butanoic acid

1.2 Other means of identification

Product number -
Other names Butanoic acid,4-((2-((2,6-dimethylphenyl)amino)-2-oxoethyl)amino)

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:123941-02-6 SDS

123941-02-6Downstream Products

123941-02-6Relevant articles and documents

Synthesis and anticonvulsant activity of 4-(2-(2,6-dimethylphenylamino)-2-oxoethylamino)-N-(substituted)butanamides: A pharmacophoric hybrid approach

Yogeeswari, Perumal,Sriram, Dharmarajan,Sahitya, Puppala,Ragavendran, Jegadeesan Vaigunda,Ranganadh, Velagaleti

, p. 3712 - 3715 (2008/02/10)

A series of pharmacophoric hybrids of ameltolide-γ-aminobutyric acid (GABA)-amides was designed, synthesized, and evaluated for their anticonvulsant and neurotoxic properties. Initial anticonvulsant screening was performed using intraperitoneal (ip) maximal electroshock-induced seizure (MES), subcutaneous pentylenetetrazole (scPTZ), and subcutaneous picrotoxin (scPIC)-induced seizure threshold tests. All the compounds had improved lipophilicity and the pharmacological activity profile confirmed their blood-brain barrier penetration. The titled compounds showed promising activity in scPIC screen indicating the involvement of GABA-mediation. Compound 4-(2-(2,6-dimethylaminophenylamino)-2-oxoethylamino)-N-(2,6-dimethylphenyl) butanamide (7) emerged as the most potent derivative effective in all the three animal models of seizure with no neurotoxicity at the anticonvulsant dose.

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