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68887-67-2

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68887-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68887-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,8 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68887-67:
(7*6)+(6*8)+(5*8)+(4*8)+(3*7)+(2*6)+(1*7)=202
202 % 10 = 2
So 68887-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2O2/c13-10(14)5-3-1-2-4-7-12-8-6-11-9-12/h6,8-9H,1-5,7H2,(H,13,14)

68887-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-imidazol-1-ylheptanoic acid

1.2 Other means of identification

Product number -
Other names 1H-Imidazole-1-heptanoic 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:68887-67-2 SDS

68887-67-2Downstream Products

68887-67-2Relevant articles and documents

Bifunctional small molecule compound capable of activating enzyme catalytic reaction, and applications thereof

-

Paragraph 0066-0068; 0072; 0075-0081; 0082-0086, (2019/10/01)

The present invention relates to a catalytic reaction, particularly to a bifunctional small molecule compound capable of activating an enzyme catalytic reaction, and applications thereof, wherein thebifunctional small molecule compound is C5-10 carboxylic acid, C5-10 fluorocarboxylic acid, aromatic heterocyclic ring substituted carboxylic acid, heterocyclic ring substituted carboxylic acid, a C5-10 carboxylic acid amide derivative, a C5-10 fluorocarboxylic acid amide derivative, an aromatic heterocyclic ring substituted carboxylic acid amide derivative or a heterocyclic ring substituted carboxylic acid amide derivative substituted with at least a catalytic group, wherein the carboxyl group or the amide derivative is used as an anchoring group. According to the present invention, with themethod, the number of the introduced catalytic groups cannot be limited, and the orientation of the catalytic functional group and the fine adjustment of the distance from the active center can be achieved, such that the H2O2 activation efficiency can be well enhanced, and the catalytic activity and the stereoselectivity can be improved.

Development of imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors

Hack, Silke,W?rlein, Babette,H?fner, Georg,Pabel, J?rg,Wanner, Klaus T.

experimental part, p. 1483 - 1498 (2011/05/11)

A new series of potential GABA uptake inhibitors starting from of 1H-imidazol-4-ylacetic acid with the carboxylic acid side chain originating from different positions and varying in length have been synthesized and tested for the inhibitory potency at the

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