Cas 1333406-08-8,5-(5-(4-(methylthio)phenethyl)-1,3,4-thiadiazol-2-yl)-1H-benzo[d]imidazole

1333406-08-8

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Basic information

Product Name: 5-(5-(4-(methylthio)phenethyl)-1,3,4-thiadiazol-2-yl)-1H-benzo[d]imidazole
Synonyms: 5-(5-(4-(methylthio)phenethyl)-1,3,4-thiadiazol-2-yl)-1H-benzo[d]imidazole
CAS NO:1333406-08-8
Molecular Formula:
Molecular Weight: 352.484
EINECS: N/A
Product Categories: N/A
Mol File: 1333406-08-8.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-(5-(4-(methylthio)phenethyl)-1,3,4-thiadiazol-2-yl)-1H-benzo[d]imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-(5-(4-(methylthio)phenethyl)-1,3,4-thiadiazol-2-yl)-1H-benzo[d]imidazole(1333406-08-8)
EPA Substance Registry System: 5-(5-(4-(methylthio)phenethyl)-1,3,4-thiadiazol-2-yl)-1H-benzo[d]imidazole(1333406-08-8)

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: 1333406-08-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333406-08-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,4,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1333406-08:
(9*1)+(8*3)+(7*3)+(6*3)+(5*4)+(4*0)+(3*6)+(2*0)+(1*8)=118
118 % 10 = 8
So 1333406-08-8 is a valid CAS Registry Number.

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1333406-08-8Relevant articles and documents

NOVEL INHIBITORS

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Page/Page column 95; 113-114, (2011/10/03)

The invention relates to novel heterocyclic derivatives as inhibitors of glutaminyl cyclase (QC, EC 2.3.2.5). QC catalyzes the intramolecular cyclization of N-terminal glutamine residues into pyroglutamic acid (5-oxo-prolyl, pGlu*) under liberation of ammonia and the intramolecular cyclization of N-terminal glutamate residues into pyroglutamic acid under liberation of water.

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