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110841-02-6

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110841-02-6 Usage

General Description

The chemical "2,3-Diazabicyclo[3.1.0]hex-2-ene-1-carboxylic acid, 6,6-dimethyl-, methyl ester (9CI)" is a compound with a complex molecular structure. It is an ester derivative of 2,3-diazabicyclo[3.1.0]hex-2-ene-1-carboxylic acid, which is a bicyclic organic compound. This chemical is commonly used in organic synthesis, particularly as a catalyst or reagent in various chemical reactions. It has applications in pharmaceutical and agrochemical industries as well. The compound's 9CI nomenclature indicates that it is listed in the preferred International Union of Pure and Applied Chemistry (IUPAC) nomenclature for chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 110841-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 110841-02:
(8*1)+(7*1)+(6*0)+(5*8)+(4*4)+(3*1)+(2*0)+(1*2)=76
76 % 10 = 6
So 110841-02-6 is a valid CAS Registry Number.

110841-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Diazabicyclo[3.1.0]hex-2-ene-1-carboxylicacid,6,6-dimethyl-,methylester(9CI)

1.2 Other means of identification

Product number -
Other names 1H-Imidazole-1-carboxylic acid,4-amino-5-cyano-,methyl ester

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:110841-02-6 SDS

110841-02-6Downstream Products

110841-02-6Relevant articles and documents

THE PREPARATION AND DECOMPOSITION OF ALKYL 2-DIAZOPENT-4-ENOATES AND 1-TRIMETHYLSILYL-1-DIAZOBUT-3-ENES

Baird, Mark S.,Hussain, Helmi H.

, p. 215 - 224 (2007/10/02)

The pyrazolines (12), (18), (21), (26) and (32), prepared by addition of diazomethane to alkyl cyclopropene-1-carboxylates or to 1-trimethylsilylcyclopropenes respectively, rearrange at 20 to 70 deg C to diazo-compounds (14), (19), (23), (28) and (36).Pyrazolines (22) and (33) are unchanged under these conditions.Catalytic decomposition of the diazo-compounds is highly dependent on the nature of the substituents and on the catalyst, leading to bicyclobutanes or dienes apparently derived by intramolecular addition, hydrogen shifts or vinyl shifts in intermediate carbenoids.In the case of (36) decomposition in the presence of rhodium acetate leads cleanly to the Z-alkene (37) while in the presence of PdCl2(CH3CN)2 the E-isomer (38) is produced.

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