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Synthesis Reference(s)

Tetrahedron Letters, 31, p. 5135, 1990 DOI: 10.1016/S0040-4039(00)97824-9

Check Digit Verification of cas no

The CAS Registry Mumber 75898-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,9 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75898-26:
(7*7)+(6*5)+(5*8)+(4*9)+(3*8)+(2*2)+(1*6)=189
189 % 10 = 9
So 75898-26-9 is a valid CAS Registry Number.

InChI:InChI=1/C5H7NO6/c6-2(5(11)12)1(3(7)8)4(9)10/h1-2H,6H2,(H,7,8)(H,9,10)(H,11,12)

75898-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2S)-2-Amino-1,1,2-ethanetricarboxylic acid

1.2 Other means of identification

Product number	-
Other names	d,l-trans-Chrysanthemsaeure-butylester

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:75898-26-9 SDS

75898-26-9Upstream product

75898-26-9Downstream Products

75898-26-9Relevant articles and documents

2-AZA-?-ALLYLPALLADIUM COMPLEXES FOR THE SYNTHESIS OF β-CARBOXYASPARTIC ACID (ASA) DERIVATIVES

O'Donnell, Martin J.,Yang, Xiaobei,Li, Min

, p. 5135 - 5138 (2007/10/02)

Reaction of malonate anions with Schiff base acetates (3) in the presence of a palladium catalyst yields protected derivatives of β-carboxyaspartic acid (5).

SYNTHESIS OF D,L-β-CARBOXYASPARTIC ACID FROM HYDANTOIN-5-MALONIC ACID DIETHYL ESTER

Henson, Edward B.,Gallop, Paul M.,Hauschka, Peter V.

, p. 2561 - 2562 (2007/10/02)

Hydantoin-5-malonic acid diethyl ester was synthesized by reduction of parabanic acid (oxalyl urea) to 5-hydroxy-hydantoin, conversion to 5-chlorohydantoin and condensation with malonic ester.Alkaline hydrolysis gave D,L-β-carboxyaspartic acid.

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75898-26-9