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53921-74-7

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53921-74-7 Usage

General Description

"(2-Acetyl-1,2,3,4-tetrahydroisoquinolin-1-yl)acetic acid" is a chemical compound that is derived from tetrahydroisoquinoline and acetic acid. It is a potential pharmacological agent with possible therapeutic applications due to its structural properties and potential pharmacological activities. The compound has a tetrahydroisoquinoline core, which is a structural motif found in a variety of biologically active compounds, and it is linked to an acetic acid moiety. (2-ACETYL-1,2,3,4-TETRAHYDROISOQUINOLIN-1-YL)ACETIC ACID may have the potential to interact with biological targets and exhibit pharmacological effects, although further research is needed to fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53921-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,2 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53921-74:
(7*5)+(6*3)+(5*9)+(4*2)+(3*1)+(2*7)+(1*4)=127
127 % 10 = 7
So 53921-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3/c1-9(15)14-7-6-10-4-2-3-5-11(10)12(14)8-13(16)17/h2-5,12H,6-8H2,1H3,(H,16,17)

53921-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-acetyl-3,4-dihydro-1H-isoquinolin-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (2-acetyl-1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetic 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:53921-74-7 SDS

53921-74-7Downstream Products

53921-74-7Relevant articles and documents

Studies on Quinoline and Isoquinoline Derivatives. VI. Addition Reaction of Diketene with Isoquinolines in the Presence of Carboxylic Acids

Yamanaka, Hiroshi,Shiraishi, Takayuki,Sakamoto, Takao,Matsuda, Hitomi

, p. 1049 - 1055 (2007/10/02)

The addition reaction of diketene in formic, acetic or propionic acid to isoquinoline afforded 1-acetonyl-2-acyl-1,2-dihydroisoquinoline (II) in satisfactory yields.Though no reaction of this type was observed to occur in quinoline, isoquinoline-like N-heteroaromatic compounds such as phthalazine and 1,6-naphthyridine underwent similar addition reactions to give the corresponding dihydro-acetonyl compounds.The above product II was easily convertible to benzoquinolizine derivatives.Keywords - diketene; mixed anhydride; isoquinoline; phthalazine; 1,6-naphthyridine; 1,2-dihydroisoquinoline

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