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37600-46-7

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37600-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37600-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,0 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37600-46:
(7*3)+(6*7)+(5*6)+(4*0)+(3*0)+(2*4)+(1*6)=107
107 % 10 = 7
So 37600-46-7 is a valid CAS Registry Number.

37600-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(naphthalen-2-ylamino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names 4-(2-naphthylamino)-4-oxobutanoic acid

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:37600-46-7 SDS

37600-46-7Relevant articles and documents

Conjugates of desferrioxamine and aromatic amines improve markers of iron-dependent neurotoxicity

Carvalho, Rodrigo R. V.,Peres, Tanara V.,Liria, Cleber W.,Machini, M. Teresa,Aschner, Michael,Espósito, Breno P.

, p. 259 - 275 (2021/01/07)

Abstract: Alzheimer’s Disease (AD) is a complex neurodegenerative disorder associated in some instances with dyshomeostasis of redox-active metal ions, such as copper and iron. In this work, we investigated whether the conjugation of various aromatic amines would improve the pharmacological efficacy of the iron chelator desferrioxamine (DFO). Conjugates of DFO with aniline (DFOANI), benzosulfanylamide (DFOBAN), 2-naphthalenamine (DFONAF) and 6-quinolinamine (DFOQUN) were obtained and their properties examined. DFOQUN had good chelating activity, promoted a significant increase in the inhibition of β-amyloid peptide aggregation when compared to DFO, and also inhibited acetylcholinesterase (AChE) activity both in vitro and in vivo (Caenorhabditis elegans). These data indicate that the covalent conjugation of a strong iron chelator to an AChE inhibitor offers a powerful approach for the amelioration of iron-induced neurotoxicity symptoms. Graphic abstract: [Figure not available: see fulltext.]

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