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120104-68-9

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120104-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120104-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,0 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 120104-68:
(8*1)+(7*2)+(6*0)+(5*1)+(4*0)+(3*4)+(2*6)+(1*8)=59
59 % 10 = 9
So 120104-68-9 is a valid CAS Registry Number.

120104-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-phenylmethoxyiminoacetate

1.2 Other means of identification

Product number -
Other names methyl glyoxylate O-benzyloxime

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:120104-68-9 SDS

120104-68-9Relevant articles and documents

Remote stereocontrol in reactions between 4- and 5-alkoxyalk-2- enylstannanes and 1-alkoxycarbonylimines and analogues: Stereoselective approaches to novel α-amino acids

Hallett, David J.,Tanikkul, Nongluk,Thomas, Eric J.

experimental part, p. 6130 - 6158 (2012/09/05)

Reactions of the allyltin trichloride 45 generated from (4S)-4-benzyloxypent-2-enyl(tributyl)stannane 1 with imines prepared from glyoxylates proceed with useful levels of 1,5-stereocontrol in favour of (4E)-2,6-anti-2-(alkylamino)-6-benzyloxyhept-4-enoat

One-pot synthesis of α-amino acids based on free radical-mediated carbon-carbon bond formation

Miyabe, Hideto,Yoshioka, Naoko,Ueda, Masafumi,Naito, Takeaki

, p. 3659 - 3660 (2007/10/03)

The one-pot reaction of 2-hydroxy-2-methoxyacetic acid methyl ester with benzyloxyamine and an alkyl radical provided a convenient method for preparing the protected α-amino acids via a carbon-carbon bond formation by intermolecular carbon radical additio

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