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124937-62-8

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124937-62-8 Usage

Uses

2-Methoxy-5-methyl-β-phenylbenzenepropanoic Acid Methyl Ester is a related compound to Tolterodine (T535795), a muscarinic receptor antagonist. Used in the treatment of urinary incontinence.

Check Digit Verification of cas no

The CAS Registry Mumber 124937-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,3 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124937-62:
(8*1)+(7*2)+(6*4)+(5*9)+(4*3)+(3*7)+(2*6)+(1*2)=138
138 % 10 = 8
So 124937-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H20O3/c1-13-9-10-17(20-2)16(11-13)15(12-18(19)21-3)14-7-5-4-6-8-14/h4-11,15H,12H2,1-3H3

124937-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(2-methoxy-5-methylphenyl)-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names Benzenepropanoic acid,2-methoxy-5-methyl-b-phenyl-,methyl ester

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:124937-62-8 SDS

124937-62-8Downstream Products

124937-62-8Relevant articles and documents

Rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids to coumarins: Asymmetric synthesis of (R)-tolterodine

Chen, Gang,Tokunaga, Norihito,Hayashi, Tamio

, p. 2285 - 2288 (2007/10/03)

(Chemical Equation Presented) Rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids to coumarins proceeded with high enantioselectivity in the presence of a rhodium catalyst (3 mol %) generated from Rh(acac)(C 2H4)2 and (R)-Segphos to give the corresponding (R)-4-arylchroman-2-ones in over 99% ee. This asymmetric reaction was applied to the synthesis of (R)-tolterodine.

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