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143361-87-9

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143361-87-9 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 29, p. 1027, 1992 DOI: 10.1002/jhet.5570290463

Check Digit Verification of cas no

The CAS Registry Mumber 143361-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,3,6 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143361-87:
(8*1)+(7*4)+(6*3)+(5*3)+(4*6)+(3*1)+(2*8)+(1*7)=119
119 % 10 = 9
So 143361-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14N2S2/c16-14-13(9-5-1-3-7-11(9)18-14)15-17-10-6-2-4-8-12(10)19-15/h2,4,6,8H,1,3,5,7,16H2

143361-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,3-benzothiazol-2-yl)-4,5,6,7-tetrahydro-1-benzothiophen-2-amine

1.2 Other means of identification

Product number -
Other names 3-Benzothiazol-2-yl-4,5,6,7-tetrahydro-benzo[b]thiophen-2-ylamine

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:143361-87-9 SDS

143361-87-9Relevant articles and documents

Novel cycloalkylthiophene-imine derivatives bearing benzothiazole scaffold: Synthesis, characterization and antiviral activity evaluation

Ke, Shaoyong,Wei, Yanhong,Yang, Ziwen,Wang, Kaimei,Liang, Ying,Shi, Liqiao

, p. 5131 - 5134 (2013/09/12)

A series of novel cycloalkylthiophene-imine derivatives containing benzothiazole unit were designed, synthesized and evaluated for their anti-viral activities. The bio-evaluation results indicated that some of the target compounds (such as 5g, 5i, 5u) exhibited good to moderate antiviral effect on CVB5, ADV7 and EV71 viruses, however, these compounds did not have inhibition activity against H1N1 virus. Especially, the compounds 4c and 4d also exhibited high antiviral activities, which provide a new and efficient approach to evolve novel multi-functional antiviral agents by rational integration of active pharmacophores.

Synthesis of 3-Hetaryl-4,5,6,7-tetrahydrobenzothiophenes

Sabnis, R. W.,Rangnekar, D. W.

, p. 1027 - 1029 (2007/10/02)

A novel efficient synthesis of 3-hetaryl-4,5,6,7-tetrahydrobenzothiophenes was achieved by the cyclocondensation of ethyl 2-amino-4,5,6,7-tetrahydrobenzothiophene-3-carboxylate with selected o-substituted aromatic amines or with alifatic, aromatic a

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