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390815-44-8

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  • AMINO-(2-METHOXY-PHENYL)-ACETIC ACID METHYL ESTER HYDROCHLORIDE

    Cas No: 390815-44-8

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390815-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 390815-44-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,0,8,1 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 390815-44:
(8*3)+(7*9)+(6*0)+(5*8)+(4*1)+(3*5)+(2*4)+(1*4)=158
158 % 10 = 8
So 390815-44-8 is a valid CAS Registry Number.

390815-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-amino-2-(2-methoxyphenyl)acetate,hydrochloride

1.2 Other means of identification

Product number -
Other names F2147-0638

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:390815-44-8 SDS

390815-44-8Downstream Products

390815-44-8Relevant articles and documents

Cobalt-Catalyzed, Directed C-H Functionalization/Annulation of Phenylglycinol Derivatives with Alkynes

Bolsakova, Jekaterina,Lukasevics, Lukass,Grigorjeva, Liene

, p. 4482 - 4499 (2020/04/09)

A new method for cobalt-catalyzed C(sp2)-H functionalization of phenylglycinol derivatives with terminal and internal alkynes directed by picolinamide auxiliary has been developed. This method offers an efficient and highly regioselective route for the synthesis of 1-hydroxymethyltetrahydroisoquinolines. The reaction employs commercially available Co(II) catalyst in the presence of Mn(III) cooxidant and oxygen as a terminal oxidant and proceeds with full preservation of original stereochemistry.

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