Welcome to LookChem.com Sign In|Join Free
  • or
N-(3-cyano-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20036-97-9

Post Buying Request

20036-97-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

20036-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20036-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,3 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20036-97:
(7*2)+(6*0)+(5*0)+(4*3)+(3*6)+(2*9)+(1*7)=69
69 % 10 = 9
So 20036-97-9 is a valid CAS Registry Number.

20036-97-9SDS

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 N-acetylglufosinate

1.2 Other means of identification

Product number -
Other names 2-acetamido-3-cyano-4,5-tetramethylenethiophene

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:20036-97-9 SDS

20036-97-9Downstream Products

20036-97-9Relevant academic research and scientific papers

Identification and optimization of small molecule antagonists of vasoactive intestinal peptide receptor-1 (VIPR1)

Harikrishnan, Lalgudi S.,Srivastava, Neelam,Kayser, Lauren E.,Nirschl, David S.,K, Kumaragurubaran,Roy, Amrita,Gupta, Anuradha,Karmakar, Sukhen,Karatt, Tajudheen,Mathur, Arvind,Burford, Neil T.,Chen, Jing,Kong, Yan,Cvijic, Maryellen,Cooper, Christopher B.,Poss, Michael A.,Trainor, George L.,Wong, Tai W.

scheme or table, p. 2287 - 2290 (2012/04/18)

Identification, synthesis and structure-activity relationship of small-molecule VIPR1 antagonists encompassing two chemical series are described.

Reactions of 2-amino-4,5,6,7-tetrahydro[1]benzothiophene-3-carbonitrile and 6-amino-1,4-dihydro-3-methyl-1,4-diphenylpyrano[2,3-c]pyrazole-5-carbonitrile with substituted benzylidenemalononitriles, α,β-acetylenic esters and ketones

Said, Ahmed,Youssef, Ahmed

experimental part, p. 214 - 217 (2009/12/03)

Reactions of 2-amino-4,5,6,7-tetrahydro[1]benzothiophene-3-carbonitrile (1a) with substituted benzylidenemalononitriles gave 4-amino-2-(1-cyano-2- arylvinyl)benzothieno[2,3-d]pyrimidine derivatives (3) as (E,Z)-mixtures and in one case (2c) as separated (

Synthesis, Antitumor and Anti-HIV-1 Testing of Certain Thieno[2,3-d]pyrimidine, Thieno[2,3-d]imidazo[1,2-c] pyrimidine and Thieno[2,3-d][1,3]thiazine Derivatives

Shehata,El-Subbagh,Abdelal,El-Sherbeny,Al-Obaid

, p. 148 - 163 (2007/10/03)

A series of tetrahydrobenzo[b]thieno[2,3-d]pyrimidines, thieno[3,2-e]imidazo[1,2-c]pyrimidines and thieno[2,3-dt][1,3]thiazines was synthesized as antitumor, antiviral agents. Compounds 2, 3 and 17 possessed moderate Anti-HIV-1 potency with EC50 values ranging from 1.83 × 10-5 to 3.42 × 10-5 molar concentrations. All of the tested compounds showed cytotoxic effects (log GI50 ≤ -4.0) against the growth of a variety of human tumor cell lines, including those derived from solid tumors. Compounds 3 and 7 showed strong potency while compounds 11 and 16 exhibited moderate activity. The detailed synthesis, spectroscopic and biological data are reported.

Derivatives of thiophene

-

, (2008/06/13)

New dicyclic thiophene compounds having the structural formula STR1 wherein X is an ester or cyano group and Y is a substituted amino group. The compounds are useful as agricultural chemicals and particularly as ripeners for sugarcane.

Use of polycyclic thiophene compounds as ripeners for sugarcane

-

, (2008/06/13)

Sucrose yield of sugarcane is increased by treating the cane crop a few weeks prior to harvest with a certain type of polycyclic thiophene compound of the formula SPC1 Wherein X is cyano, carboalkoxy or carbamido and Y is an amino or substituted amino group, or with mixtures comprising one or more such compounds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 20036-97-9