Cas 1244641-08-4,N-{3-[5-(2-chloro-4-pyrimidinyl)-2-ethyl-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

1244641-08-4

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Basic information

Product Name: N-{3-[5-(2-chloro-4-pyrimidinyl)-2-ethyl-1,3-thiazol-4-yl]phenyl}benzenesulfonamide
Synonyms: N-{3-[5-(2-chloro-4-pyrimidinyl)-2-ethyl-1,3-thiazol-4-yl]phenyl}benzenesulfonamide
CAS NO:1244641-08-4
Molecular Formula:
Molecular Weight: 456.977
EINECS: N/A
Product Categories: N/A

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: N-{3-[5-(2-chloro-4-pyrimidinyl)-2-ethyl-1,3-thiazol-4-yl]phenyl}benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{3-[5-(2-chloro-4-pyrimidinyl)-2-ethyl-1,3-thiazol-4-yl]phenyl}benzenesulfonamide(1244641-08-4)
EPA Substance Registry System: N-{3-[5-(2-chloro-4-pyrimidinyl)-2-ethyl-1,3-thiazol-4-yl]phenyl}benzenesulfonamide(1244641-08-4)

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: 1244641-08-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1244641-08-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,6,4 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1244641-08:
(9*1)+(8*2)+(7*4)+(6*4)+(5*6)+(4*4)+(3*1)+(2*0)+(1*8)=134
134 % 10 = 4
So 1244641-08-4 is a valid CAS Registry Number.

1244641-08-4Upstream product

631-58-3 thiopropanamide

1244641-08-4Downstream Products

1244641-03-9 N-{3-[2-ethyl-5-(2-{[3,4,5-tris(methyloxy)phenyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

1244641-08-4Relevant academic research and scientific papers

THIAZOLE SULFONAMIDE AND OXAZOLE SULFONAMIDE KINASE INHIBITORS

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Page/Page column 113-114, (2010/10/03)

The present invention provides thiazole sulfonamide and oxazole sulfonamide compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents

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