Cas 610316-03-5,Acetic acid, (3-ethyl-2(3H)-benzothiazolylidene)-, (2Z)- (9CI)

610316-03-5

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Basic information

Product Name: Acetic acid, (3-ethyl-2(3H)-benzothiazolylidene)-, (2Z)- (9CI)
Synonyms: Acetic acid, (3-ethyl-2(3H)-benzothiazolylidene)-, (2Z)- (9CI)
CAS NO:610316-03-5
Molecular Formula: C11H11NO2S
Molecular Weight: 221.27554
EINECS: N/A
Product Categories: ETHYL
Mol File: 610316-03-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetic acid, (3-ethyl-2(3H)-benzothiazolylidene)-, (2Z)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid, (3-ethyl-2(3H)-benzothiazolylidene)-, (2Z)- (9CI)(610316-03-5)
EPA Substance Registry System: Acetic acid, (3-ethyl-2(3H)-benzothiazolylidene)-, (2Z)- (9CI)(610316-03-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 610316-03-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 610316-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,3,1 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 610316-03:
(8*6)+(7*1)+(6*0)+(5*3)+(4*1)+(3*6)+(2*0)+(1*3)=95
95 % 10 = 5
So 610316-03-5 is a valid CAS Registry Number.

610316-03-5Upstream product

610315-94-1 (3-ethyl-3H-benzothiazol-2-ylidene)-acetic acid ethyl ester

610316-03-5Downstream Products

610316-03-5Relevant articles and documents

Synthesis and PDF inhibitory activities of novel benzothiazolylidenehydroxamic acid derivatives

Takayama, Wataru,Shirasaki, Yoshihisa,Sakai, Yusuke,Nakajima, Emi,Fujita, Shuhei,Sakamoto-Mizutani, Kanako,Inoue, Jun

, p. 3273 - 3276 (2007/10/03)

A novel series of benzothiazolylidenehydroxamic acid derivatives has been designed and synthesized as PDF inhibitors. Some of this novel class of PDF inhibitors exhibited micromolar order enzyme inhibitory activity and antibacterial activity.

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