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3806-02-8

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3806-02-8 Usage

General Description

Diethyl-2-aminoazulene-1,3-dicarboxylate is a chemical compound with the molecular formula C14H16N2O4. It is a derivative of azulene, a bicyclic aromatic hydrocarbon, and contains two ester groups and an amino group. DIETHYL-2-AMINOAZULENE-1,3-DICARBOXYLATE is commonly used in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceuticals and other biologically active molecules. Its unique structure and properties make it an important intermediate in the production of drugs and other fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 3806-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3806-02:
(6*3)+(5*8)+(4*0)+(3*6)+(2*0)+(1*2)=78
78 % 10 = 8
So 3806-02-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO4/c1-3-20-15(18)12-10-8-6-5-7-9-11(10)13(14(12)17)16(19)21-4-2/h5-9H,3-4,17H2,1-2H3

3806-02-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-aminoazulene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1,3-diethoxycarbonyl-2-aminoazulene

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:3806-02-8 SDS

3806-02-8Relevant articles and documents

Asymmetric synthesis and characterization of chiral 2,2′-diamino-3, 3′-diethoxycarbonyl-8,8′-diphenyl-1,1′-biazulene

Chen, Arh-Hwang,Yen, Hsiu-Hang,Kuo, Yu-Chen,Chen, Wen-Zhang

, p. 2975 - 2987 (2008/02/12)

rac-2,2′-Diamino-3,3′-diethoxycarbonyl-8,8′-diphenyl-1, 1′-biazulene was synthesized from diethyl 2-aminoazulene-1,3-dicarboxylate and was optically resolved into two enantiomers of S-form and R-form. The enantioselective oxidative couplings with two chir

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