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1H-Benz[g]indazole-3-carboxylic acid, 4,5-dihydro-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60656-32-8

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60656-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60656-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,5 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60656-32:
(7*6)+(6*0)+(5*6)+(4*5)+(3*6)+(2*3)+(1*2)=118
118 % 10 = 8
So 60656-32-8 is a valid CAS Registry Number.

60656-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-4,5-dihydro-1H-benzo[g]indazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Phenyl-4,5-dihydrobenz[g]indazole-3-carboxylic acid

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:60656-32-8 SDS

60656-32-8Relevant academic research and scientific papers

Cycloaddition of Nitrile Imines with Enamides: An Approach to Functionalized Pyrazolines and Pyrazoles

Tu, Liang,Gao, Limei,Wang, Xiaomeng,Shi, Ruijie,Ma, Rupei,Li, Junfei,Lan, Xiaoshuang,Zheng, Yongsheng,Liu, Jikai

, p. 559 - 573 (2021)

An efficient [3 + 2] cycloaddition of in situ generated nitrile imines with enamides has been established. A wide range of functionalized pyrazoline derivatives (53 examples) were obtained in moderate to good yields (up to 96%) under very mild conditions. This protocol features broad substrate scope, good functional group tolerance, and operational simplicity. Practical transformation of the products into useful pyrazoles via a one-pot process and the scalability of this protocol highlight the utility of this synthetic methodology.

3-AMIDOPYRAZOLE DERIVATIVES, PROCESS FOR PREPARING THESE AND PHARMACEUTICAL COMPOSITES CONTAINING THEM

-

, (2008/06/13)

The present invention relates to new pyrazole derivatives possessing an amide group substituted with an amino acid or one of its derivatives at position 3 and variously substituted in positions 1, 2, 4 or 5 of the pyrazole ring, to a process for preparing these and to pharmaceutical compositions containing the said pyrazole derivatives as an active ingredient.

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