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123673-31-4

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123673-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123673-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,6,7 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123673-31:
(8*1)+(7*2)+(6*3)+(5*6)+(4*7)+(3*3)+(2*3)+(1*1)=114
114 % 10 = 4
So 123673-31-4 is a valid CAS Registry Number.

123673-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-3-(benzyloxycarbonylamino)-4-hydroxybutanoic acid

1.2 Other means of identification

Product number -
Other names -

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:123673-31-4 SDS

123673-31-4Relevant articles and documents

INHIBITING B-CELL LYMPHOMA 2 (BCL-2) AND RELATED PROTEINS

-

Paragraph 00125, (2017/09/05)

Novel compounds inhibiting anti-apoptosis proteins B-cell lymphoma 2 (Bcl-2) and Bcl-XL include compounds of formula (I) and formula (II) disclosed herein, as well as liposome compositions comprising Bcl-2 inhibitor compounds. These compositions are usefu

Highly Diastereoselective 1,4-Addition of Amines to Chiral α,β-Unsaturated δ-Lactone

Yoda, Hidemi,Shirai, Tsuyoshi,Kawasaki, Tomoyasu,Katagiri, Takao,Takabe, Kunihiko,et al.

, p. 793 - 794 (2007/10/02)

Michael addition of amines to (S)-γ-amino-α,β-unsaturated δ-lactones was accomplished in extremely high diastereoselectivity with the ring-opening reactions and was disclosed to furnish (3R,4S)-diamino-hydroxyamides in high yields.

Selective Reduction of Nα-Protected Dicarboxylic Amino Acid Anhydrides into Corresponding Protected Amino Alcohols

Kundu, B.,Srivastava, V. P.,Mathur, K. B.

, p. 1124 (2007/10/02)

Nα-Protected dicarboxylic amino acid anhydrides, such as those of Z-D-Asp or Z-D-Glu have been selectively reduced in excellent yields with NaBH4 to give the corresponding Nα-protected amino alcohols.A probable mechanism for the sele

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