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Cyclohexanecarboxylic acid, 4-amino-, phenylmethyl ester, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67299-44-9

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67299-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67299-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,9 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67299-44:
(7*6)+(6*7)+(5*2)+(4*9)+(3*9)+(2*4)+(1*4)=169
169 % 10 = 9
So 67299-44-9 is a valid CAS Registry Number.

67299-44-9SDS

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 Benzyl-cis-4-aminocyclohexancarboxylat

1.2 Other means of identification

Product number -
Other names -

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:67299-44-9 SDS

67299-44-9Relevant academic research and scientific papers

ORGANIC ARSENIC-BASED TYPE II PYRUVATE KINASE INHIBITOR AS WELL AS PREPARATION METHOD THEREFOR AND USE THEREOF

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, (2022/04/08)

Provided by the present invention are an organic arsenic-based type II pyruvate kinase inhibitor as well as a preparation method therefor and a use thereof. Specifically, a PKM2 inhibitor of the present invention is a compound represented by formula I, or a pharmaceutically acceptable salt thereof, or a stereoisomer or tautomer, a hydrate or a solvate thereof, wherein, X1, X2, R1, R2, R3, R4, R5 and n are as defined in the description. The compound of the present invention has a high inhibitory activity and high specificity for PKM2 and is well suited for the preparation of a drug inhibiting tumors by inhibiting a PKM2 pathway.

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