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100860-96-6

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100860-96-6 Usage

Classification

dissociative anesthetic

Medical uses

anesthesia, sedation

Mechanism of action

blocks the effects of the neurotransmitter glutamate in the brain

Effects

dissociative anesthesia, analgesia

Other potential uses

antidepressant, anti-inflammatory, depression, chronic pain

Risks

potential for abuse, recreational use, addiction.

Check Digit Verification of cas no

The CAS Registry Mumber 100860-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100860-96:
(8*1)+(7*0)+(6*0)+(5*8)+(4*6)+(3*0)+(2*9)+(1*6)=96
96 % 10 = 6
So 100860-96-6 is a valid CAS Registry Number.

100860-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethylamino)-1-thiophen-3-ylpropan-1-one

1.2 Other means of identification

Product number -
Other names -

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:100860-96-6 SDS

100860-96-6Relevant articles and documents

Synthesis of 2,6-diaryl-substituted pyridines and their antitumor activities

Son, Jong-Keun,Zhao, Long-Xuan,Basnet, Arjun,Thapa, Pritam,Karki, Radha,Na, Younghwa,Jahng, Yurngdong,Jeong, Tae Cheon,Jeong, Byeong-Seon,Lee, Chong-Soon,Lee, Eung-Seok

, p. 675 - 682 (2008)

For the development of novel antitumor agents, we designed and synthesized 2,6-diaryl-substituted pyridine derivatives bearing three aryl groups, which are the bioisosteres of terpyridine, and evaluated their biological activities. Most of the 18 prepared compounds showed moderate cytotoxicity against several human cancer cell lines. From the structure-activity relationships we may conclude that the number of aryl groups employed would be critical for their biological activities.

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