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2655-37-0

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2655-37-0 Usage

Chemical Family

Pyrazole family

Physical State

Colorless liquid

Primary Use

Research and development

Applications

Pharmaceutical and agrochemical industries

Role in Synthesis

Building block or intermediate in the synthesis of various organic compounds

Hazardous Nature

Potentially hazardous

Handling and Storage

Must be done with care and in accordance with safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 2655-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2655-37:
(6*2)+(5*6)+(4*5)+(3*5)+(2*3)+(1*7)=90
90 % 10 = 0
So 2655-37-0 is a valid CAS Registry Number.

2655-37-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-3,5-dimethylpyrazole

1.2 Other means of identification

Product number -
Other names 3,5-Dimethyl-1-butylpyrazole

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:2655-37-0 SDS

2655-37-0Downstream Products

2655-37-0Relevant articles and documents

Diazirines as potent electrophilic Nitrogen sources: Application to the synthesis of Pyrazoles

Schneider, Yoann,Prévost, Julie,Gobin, Ma?lle,Legault, Claude Y.

supporting information, p. 596 - 599 (2014/04/03)

Even after more than 50 years since its discovery, the electrophilic potential of diazirines was never truly exploited. This longstanding limitation has been resolved. N-Monosubstituted diaziridines and hydrazones are obtained by nucleophilic additions. They release, under hydrolysis conditions, the corresponding monosubstituted hydrazines. The latter were converted to pyrazoles in high yields. The adamantanone can be recovered in 80-100% yields. This work demonstrates the potential of diazirines as electrophilic nitrogen sources with recoverable protecting groups.

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