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25462-38-8

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25462-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25462-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,6 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25462-38:
(7*2)+(6*5)+(5*4)+(4*6)+(3*2)+(2*3)+(1*8)=108
108 % 10 = 8
So 25462-38-8 is a valid CAS Registry Number.

25462-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-phenylpropyl)propane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2-(3-Phenylpropyl)-1,3-propanediol

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:25462-38-8 SDS

25462-38-8Relevant articles and documents

Lipase-mediated preparation of optically active isomers of Rosaphen

Kawasaki, Masashi,Toyooka, Naoki,Saka, Tomoki,Goto, Michimasa,Matsuya, Yuji,Kometani, Tadashi

experimental part, p. 135 - 142 (2010/12/20)

The optically active isomers of Rosaphen (RS)-1 were synthesized from the chiral intermediate prepared by lipase-catalyzed desymmetrization of prochiral diol. The results of an olfactory evaluation of the prepared isomers are reported.

Certain 2-substituted 1,3-propylidenediphosphonate derivatives, pharmaceutical compositions containing them and their use as antihypertensive agents

-

, (2008/06/13)

2-Substituted-1,3-propylidenediphosphonates of formula (I), where A, R1 and R2 are defined in claim 1, are therapeutically active compounds, namely for the treatment of cardiovascular diseases. They can be prepared by reacting phosphonating agents with 1,3- dibromopropanes or ditosylates of 1,3-propanediols substituted in position 2. STR1 .

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