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501361-99-5

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501361-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501361-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,3,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 501361-99:
(8*5)+(7*0)+(6*1)+(5*3)+(4*6)+(3*1)+(2*9)+(1*9)=115
115 % 10 = 5
So 501361-99-5 is a valid CAS Registry Number.

501361-99-5SDS

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 2-(4-fluorophenyl)-4-(iodomethyl)oxazole

1.2 Other means of identification

Product number -
Other names 2-(4-fluorophenyl)oxazol-4-ylmethyl iodide

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:501361-99-5 SDS

501361-99-5Relevant articles and documents

COMPOUNDS AND METHODS for the inhibition of HDAC

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Paragraph 0603-0604; 0664-0665, (2015/11/24)

Disclosed are compounds having the formula: wherein X1, X2, X3, R1, R2, R3, R4, Y, A, Z, L and n are as defined herein, and methods of making and using the same.

Diarylcycloalkyl derivatives, processes for their preparation and their use as pharmaceuticals

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, (2008/06/13)

Diarylcycloalkyl derivatives and their physiologically acceptable salts and physiologically functional derivatives are disclosed. The compounds include those of formula I, in which the radicals are as defined, and their physiologically acceptable salts an

Process for preparing the enantiomeric forms of cis-configured 1,3-cyclohexanediol derivatives

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Page 18, (2010/02/08)

Process for preparing the enantiomeric forms of cis-configured 1,3-cyclohexanediol derivatives A process is described for preparing chiral, nonracemic, cis-configured 1,3-disubstituted cyclohexanols of the formula (I) where the radicals are as defined, by

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