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37466-90-3

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37466-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37466-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,6 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37466-90:
(7*3)+(6*7)+(5*4)+(4*6)+(3*6)+(2*9)+(1*0)=143
143 % 10 = 3
So 37466-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O2/c1-2-13-9(12)6-3-4-7(10)8(11)5-6/h3-5H,2,10-11H2,1H3

37466-90-3 Well-known Company Product Price

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  • Alfa Aesar

  • (A17236)  Ethyl 3,4-diaminobenzoate, 97%   

  • 37466-90-3

  • 1g

  • 241.0CNY

  • Detail
  • Alfa Aesar

  • (A17236)  Ethyl 3,4-diaminobenzoate, 97%   

  • 37466-90-3

  • 5g

  • 1147.0CNY

  • Detail
  • Alfa Aesar

  • (A17236)  Ethyl 3,4-diaminobenzoate, 97%   

  • 37466-90-3

  • 25g

  • 2994.0CNY

  • Detail

37466-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3,4-diaminobenzoate

1.2 Other means of identification

Product number -
Other names 4-ethoxycarbonyl-o-phenylenediamine

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:37466-90-3 SDS

37466-90-3Relevant articles and documents

Synthesis and properties of alkyl chain substituted naphthalenetetracarboxylic monoanhydride monoimides and unsymmetrically substituted naphthalene derivatives

Koz, Banu,Demic, Serafettin,Icli, Siddik

, p. 2755 - 2758 (2016)

1,4,5,8-Naphthalenedianhydride is converted to N-(2-ethylhexyl)-1,4,5,8-naphthalenetetracarboxylic monoanhydride monoimide (2a) and N-(2-hydroxyethyl)-1,4,5,8-naphthalenetetracarboxylic monoanhydride monoimide (2c) through the potassium salt prepared from

Amide and ester derivatives of chlorido[4-carboxy-1,2-disalicylideneaminobenzene]iron(iii) as necroptosis and ferroptosis inducers

Baecker, Daniel,Gust, Ronald,H?rschl?ger, Carina,Kircher, Brigitte,Ma, Benjamin N.,Sagasser, Jessica,Schultz, Lukas,Steiner, Lucy,Weinreich, Maria

supporting information, p. 6842 - 6853 (2020/06/08)

In continuation of the structure-activity study about 4-substituted chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(iii) complexes as necroptosis and ferroptosis inducers, we introduced a 4-COOH group at the 1,2-phenylenediamine moiety of the lead

BENZOIMIDAZOLE DERIVATIVES AS ANTICANCER AGENTS

-

Page/Page column 39, (2018/04/20)

The invention relates to benzoimidazole derivatives, acting as anticancer drugs, as well as pharmaceutical composition containing said compounds. These compounds are able to firstly inhibit the protein/protein interactions of the MAP Kinase Erk, leading t

COMPOUND AND METHOD FOR INHIBITING SIRTUIN ACTIVITIES

-

, (2017/01/26)

A compound of formula wherein R1 is selected from the group consisting of hydrogen, halogen, hydroxyl, carboxyl, alkyl of up to 5 carbon atoms, imidazolyl, piperazinyl, morpholinyl, benzyl, R4OH or R4COOH, where R4 is (CH2)m and m is an integer of from 1 to 4; R2 is selected from the group consisting of hydrogen, phenyl or 3-(2-oxopyrrolidin-l-yl) propyl; and R3 is hydrogen or alkyl of from 1-4 carbon atoms.

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