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216392-66-4

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216392-66-4 Usage

General Description

1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-(9CI) is a chemical compound with the molecular formula C8H11NO3. It belongs to the group of pyrrolizine derivatives and is characterized by its aromatic ring structure. 1H-Pyrrolizine-7a(5H)-carboxylicacid,tetrahydro-3-oxo-(9CI) has potential applications in the field of pharmaceuticals, as it exhibits biological activities that may be useful for drug development. Its tetrahydro-3-oxo group is of particular interest, as it can undergo various chemical reactions to produce derivatives with unique properties. Further research and investigation into the biological and chemical properties of 1H-Pyrrolizine-7a(5H)-carboxylic acid, tetrahydro-3-oxo-(9CI) could lead to new developments in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 216392-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,3,9 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 216392-66:
(8*2)+(7*1)+(6*6)+(5*3)+(4*9)+(3*2)+(2*6)+(1*6)=134
134 % 10 = 4
So 216392-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO3.ClH/c10-6-2-5-9-4-1-3-8(6,9)7(11)12;/h1-5H2,(H,11,12);1H

216392-66-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolizine-7a(5H)-carboxylicacid,tetrahydro-3-oxo-(9CI)

1.2 Other means of identification

Product number -
Other names tetrahydro-3-oxo

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:216392-66-4 SDS

216392-66-4Downstream Products

216392-66-4Relevant articles and documents

Intramolecular catalysis of amide isomerization: Kinetic consequences of the 5-NH- -N(a) hydrogen bond in prolyl peptides

Cox, Christopher,Lectka, Thomas

, p. 10660 - 10668 (1998)

The presence of an intramolecular hydrogen bond has been proposed to play a key role in the catalysis of amide isomerization by peptidylprolyl isomerases (PPIases), which are highly conserved and ubiquitous rotamase enzymes that catalyze the cis-trans iso

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