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41148-79-2

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41148-79-2 Usage

General Description

N-Acetyl-L-aspartic acid anhydride is a chemical species that originates from N-acetyl-L-aspartic acid. This particular derivative is known for its significant role in mammalian brain metabolism, where it acts as a molecule involved in maintaining myelin - a fatty substance that ensures effective nerve signal transmission. It's also used as a concentration marker for NMR spectroscopy assessments due to its high concentration in human brain. Outside of medical contexts, little is known about its general uses or properties, although it's known to be an anhydride, meaning it's a compound derived from another by the removal of a water molecule.

Check Digit Verification of cas no

The CAS Registry Mumber 41148-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,4 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41148-79:
(7*4)+(6*1)+(5*1)+(4*4)+(3*8)+(2*7)+(1*9)=102
102 % 10 = 2
So 41148-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO4/c1-3(8)7-4-2-5(9)11-6(4)10/h4H,2H2,1H3,(H,7,8)/t4-/m0/s1

41148-79-2SDS

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 N-(2,5-Dioxooxolan-3-yl)acetamide

1.2 Other means of identification

Product number -
Other names N-Acetyl-L-asparaginsaeure-anhydrid

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:41148-79-2 SDS

41148-79-2Relevant articles and documents

Method for preparing enantiomerically pure 4-pyrrolidinophenylbenzyl ether derivatives

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Page/Page column 4-5, (2008/06/13)

The invention relates to a method for preparing enantiomerically pure 4-pyrrolidinophenylbenzyl ether derivatives of formula I: wherein R1, R21, R22, R23, R24 and n are as defined the description and claims and to intermediates and salts thereof useful in the method of the invention.

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