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60456-14-6

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60456-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60456-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,5 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60456-14:
(7*6)+(6*0)+(5*4)+(4*5)+(3*6)+(2*1)+(1*4)=106
106 % 10 = 6
So 60456-14-6 is a valid CAS Registry Number.

60456-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name erythro-2-bromo-3-methoxy-3-phenylpropanoic acid

1.2 Other means of identification

Product number -
Other names (2RS,3RS)-2-Brom-3-methoxy-3-phenyl-propionsaeure

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:60456-14-6 SDS

60456-14-6Relevant articles and documents

Methoxybromination of Cinnamic Acid by N-Bromosuccinimide

Karunakaran, C.,Venkatachalapathy, C.

, p. 2404 - 2407 (1990)

With cinnamic acid in aqeous methanol N-bromosuccinimide yields 2-bromo-3-methoxy-3-phenyl-propionic acid.It is a second-order reaction independent of +> at moderately high +>.At low +> the rate increases with decrea

Methoxybromination of Cinnamic Acid by IV-Bromosuccinimide

Karunakaran,Venkatachalapathy

, p. 2404 - 2407 (2017/08/15)

With cinnamic acid in aqueous methanol iV-bromosuccinimide yields 2-bromo-3-methoxy-3-phenyl-propionic acid. It is a second-order reaction independent of [H+] at moderately high [H+]. At low [H+] the rate increases with decrease in [H+]. The reaction is inhibited by succinimide. The reaction rate decreases with increase in methanol content of the medium. Mechanistic pathways of the reaction are discussed and a rate equation is derived.

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