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25462-37-7

25462-37-7

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25462-37-7 Usage

Chemical Properties

White Solid

Uses

Intermediate in the preparpation of Meprobamate (M227750) and its metabolites.

Check Digit Verification of cas no

The CAS Registry Mumber 25462-37-7 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 25462-37:
(7*2)+(6*5)+(5*4)+(4*6)+(3*2)+(2*3)+(1*7)=107
107 % 10 = 7
So 25462-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-3-4-7(2,5-8)6-9/h3,8-9H,1,4-6H2,2H3

25462-37-7SDS

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-methyl-2-prop-2-enylpropane-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,3-Propanediol,2-allyl-2-methyl

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:25462-37-7 SDS

25462-37-7Downstream Products

25462-37-7Relevant articles and documents

Enantiopure hydroxymethylated cycloalkenols as privileged small molecular multifunctional scaffolds for the asymmetric synthesis of carbocycles

Kumar, Rajan,Rej, Rohan Kalyan,Halder, Joydev,Mandal, Haridas,Nanda, Samik

, p. 498 - 512 (2016)

Enantiopure hydroxymethylated cycloalkenols bearing a quaternary stereocenter have been synthesized by a Pybox mediated enantioselective desymmetrization method. The synthesized cycloalkenols serve as starting precursors for the construction of several ch

Total synthesis of (+/-)-acetomycin and design of esterase-resistant analogs.

Uenishi,Kobayashi,Komine,Okadai,Yonemitsu,Sasaki,Yamada

, p. 517 - 523 (2007/10/03)

The synthesis of acetomycin and related analogs was investigated. Acetomycin was synthesized from diethyl allyl(methyl)malonate in 6.5% yield over 18 steps. The total number of steps was improved compared to our previous synthesis; i.e., four steps shorte

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