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58611-62-4

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58611-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58611-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,1 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58611-62:
(7*5)+(6*8)+(5*6)+(4*1)+(3*1)+(2*6)+(1*2)=134
134 % 10 = 4
So 58611-62-4 is a valid CAS Registry Number.

58611-62-4SDS

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 benzyl DL-N-(benzyloxycarbonyl)homoserinate

1.2 Other means of identification

Product number -
Other names benzyl 2-benzyloxycarbonylamino-4-hydroxybutanoate

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:58611-62-4 SDS

58611-62-4Relevant articles and documents

Inhibitors or bone reabsorption and antagonists of vitronectin receptors

-

, (2008/06/13)

Novel inhibitors of bone reabsorption and antagonists of vitronectin receptors The present invention relates to 5-membered ring heterocycles of the formula I, in which E, F, G, W, Y and Z have the meaning given in the patent claims, to their preparation a

Synthesis of D,L-&γ-Hydroxyphosphinothricin, a Potent New Inhibitor of Glutamine Synthetase

Walker, Daniel M.,McDonald, John F.,Logusch, Eugene W.

, p. 1710 - 1711 (2007/10/02)

A flexible synthesis of D,L-γ-hydroxyphosphothricin (GHPPT), a potent inhibitor of the enzyme glutamine synthetase, is described which features silicon-mediated addition of ethyl methylphosphinate to benzyl 2-benzyloxycarbonylamino-4-oxobutyrate; selectiv

Analogues of S adenosylhomocysteine as potential inhibitors of biological transmethylation. Synthesis of analogues with modifications at the 5' thioether linkage

Chang,Coward

, p. 684 - 691 (2007/10/06)

The synthesis of S adenosylhomocysteine analogues, in which the 5' thioether linkage is replaced by an oxygen or nitrogen isostere, has been investigated. These compounds were designed to be resistant to enzyme catalyzed hydrolytic cleavage of the 5' subs

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