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233261-72-8

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233261-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 233261-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,2,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 233261-72:
(8*2)+(7*3)+(6*3)+(5*2)+(4*6)+(3*1)+(2*7)+(1*2)=108
108 % 10 = 8
So 233261-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O/c13-9-10-1-3-11(4-2-10)12(15)5-7-14-8-6-12/h1-4,14-15H,5-8H2

233261-72-8SDS

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 4-(4-hydroxypiperidin-4-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names 4-(4-CYANOPHENYL)-4-HYDROXYPIPERIDINE

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:233261-72-8 SDS

233261-72-8Upstream product

233261-72-8Downstream Products

233261-72-8Relevant articles and documents

INDOLE DERIVATIVE AND USE FOR TREATMENT OF CANCER

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Page/Page column 255, (2010/02/15)

The present invention relates to a compound represented by the formula (I’) wherein A is a benzene ring optionally having substituents, R1, R2a and R3 are each a hydrogen atom, a hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, R1 and R2a may form a ring via X, when R1 and R2a form a ring via X, R1 and R2a are each a bond or a divalent C1-5 acyclic hydrocarbon group optionally having substituents, and X is a bond, an oxygen atom, an optionally oxidized sulfur atom or an imino group optionally having a substituent, provided that R1, R2a and X are not bonds at the same time, or a salt thereof, and an agent for inhibiting kinase (phosphorylation enzyme), which contains this compound or a prodrug thereof. The compound of the present invention has an inhibitory activity against kinase such as a vascular endothelial growth factor receptor (VEGFR) and the like, and is useful as an agent for the prophylaxis or threatment of cancer and the like.

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