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92403-94-6

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92403-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92403-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,0 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92403-94:
(7*9)+(6*2)+(5*4)+(4*0)+(3*3)+(2*9)+(1*4)=126
126 % 10 = 6
So 92403-94-6 is a valid CAS Registry Number.

92403-94-6SDS

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-methyl-3-phenoxypropan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Propanol,2-methyl-3-phenoxy

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:92403-94-6 SDS

92403-94-6Downstream Products

92403-94-6Relevant articles and documents

Stereocontrolled intramolecular meta-arene-alkene photocycloaddition reactions using chiral tethers: Efficiency of the tether derived from 2,4-pentanediol

Sugimura, Takashi,Yamasaki, Akiko,Okuyama, Tadashi

, p. 675 - 683 (2007/10/03)

Photochemical reactions of substrates consisting of phenyl and vinyl groups, which are tethered with a chiral diol, resulted in intramolecular meta-arene-alkene cycloaddition; the reaction efficiency as well as the stereoselectivity was studied. 1,3-Butanediol, 2-substituted 1,3-propanediols, 2-methyl-2,4-penetanediol, and 2,6-dimethyl-3,5-heptanediol were employed as tethers, and the results are compared with those obtained with 2,4-pentanediol (PD) tether, which are known to show high stereoselectivity and moderate efficiency. All the reactions with the lower analogues were less efficient than with PD, although one of the butanediol-tethered reactions afforded a single stereoisomer as PD did. The dimethylheptanediol tether showed similar efficiency but lower stereoselectivity than PD. The results suggest that the PD tether has an optimized structure having a proper flexibility.

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