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24852-71-9

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24852-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24852-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,5 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24852-71:
(7*2)+(6*4)+(5*8)+(4*5)+(3*2)+(2*7)+(1*1)=119
119 % 10 = 9
So 24852-71-9 is a valid CAS Registry Number.

24852-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(phenylmethyl)thio]benzaldehyde

1.2 Other means of identification

Product number -
Other names 2-(benzylthio)benzaldehyde

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:24852-71-9 SDS

24852-71-9Relevant articles and documents

Synthesis and characterization of triosmium clusters containing the 2-(benzylthio)benzoyl ligand

Lee, Siu-Ming,Cheung, Kung-Kai,Wong, Wing-Tak

, p. 273 - 278 (1995)

Reaction of with an equimolar proportion of 2-(benzylthio)-benzaldehyde (1) gives three new compounds: two yellow isomers of (2a and 2b) and an orange crystalline compound (3).The mol

Compounds Having CRTH2 Antagonist Activity

-

Page/Page column 13, (2010/02/17)

Compounds of general formula (I) W is chloro or fluoro; Z is a —SO2YR1 group wherein R1 is C3-C8 heterocyclyl, aryl or heteroaryl any of which may optionally be substituted with one or more substituents selected from halo, —CN, —C1-C6 alkyl, —SOR3, —SO2R3, —SO2N(R2)2, —N(R2)2, —NR2C(O)R3, —CO2R2, —CONR2R3, —NO2, —OR2, —SR2, —O(CH2)pOR2, and —O(CH2)pO(CH2)qOR2 wherein each R2 is independently hydrogen, —C1-C6 alkyl, —C3-C8 cycloalkyl, aryl or heteroaryl;each R3 is independently, —C1-C6 alkyl, —C3-C8 cycloalkyl, aryl or heteroaryl;p and q are each independently an integer from 1 to 3; Y is a straight or branched C1-C4 alkylene chain; and their pharmaceutically acceptable salts, hydrates, solvates, complexes or prodrugs are useful in orally administrable compositions for the treatment of allergic diseases such as asthma, allergic rhinitis and atopic dermatitis.

Preparation and structure of some sulfanylpropenylidene derivatives of Meldrum's acid

Crawford, Lynne A.,Mcnab, Hamish

experimental part, p. 995 - 1009 (2010/03/01)

Condensation of Meldrum's acid with the 3-sulfanylpropenal derivatives 7a and 7b gives the 3-sulfanylpropenylidene derivatives 2a and 2b, respectively. NMR and X-ray analysis of 2a and 2b show that the electron-donating group conjugates with the electron-

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