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4-methyl hydrogen DL-aspartate is a chemical compound derived from the amino acid aspartate, featuring a methyl group and a hydrogen atom attached to its carbon atom. 4-methyl hydrogen DL-aspartate holds potential in various fields, including pharmaceuticals, food additives, and research, and is recognized for its role in neurotransmission and neurological function.

1835-51-4

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1835-51-4 Usage

Uses

Used in Pharmaceutical Industry:
4-methyl hydrogen DL-aspartate is used as a building block in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Food Additive Industry:
In the food additive industry, 4-methyl hydrogen DL-aspartate serves as a source of aspartate in nutritional supplements, enhancing the nutritional value of food products.
Used in Research:
4-methyl hydrogen DL-aspartate is utilized in neuroscience research for its potential role in neurotransmission and neurological function, aiding in the study of brain mechanisms and the development of treatments for neurological disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 1835-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1835-51:
(6*1)+(5*8)+(4*3)+(3*5)+(2*5)+(1*1)=84
84 % 10 = 4
So 1835-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4/c1-10-4(7)2-3(6)5(8)9/h3H,2,6H2,1H3,(H,8,9)

1835-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl hydrogen DL-aspartate

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:1835-51-4 SDS

1835-51-4Relevant academic research and scientific papers

Urea derivatives, their preparation and medicinal products containing them

-

, (2008/06/13)

Compounds of formula: STR1 in which R1 represents an alkyl radical, R2 represents a phenyl radical or a chain --(CH2)m --R4 in which m is equal to 0, 1 or 2 and R, represents a hydroxyl, alkoxy or amino radical, R3 represents a hydrogen atom or an alkyl, alkoxy or alkylthio radical and n is equal to 0 or 1, their preparation and medicinal products containing them.

NEW SYNTHESIS OF DL-α-AMINOACIDS FROM t-BUTYL N(DIPHENYLMETHYLENE) OXAMATE

Bazureau, J.P.,Person, D.,Corre, M. Le

, p. 3065 - 3068 (2007/10/02)

The condensation of phosphorus ylids with t-butyl N(diphenylmethylene) oxamate gives 2-aza 1,3-dienes ; subsequent reduction with sodium cyanoborohydride provides protected α-aminoacids.

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