Cas 1235550-95-4,8-cyclopropyl-7-naphthalen-1-ylmethyl-5-oxo-2-p-tolyl-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester

1235550-95-4

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Basic information

Product Name: 8-cyclopropyl-7-naphthalen-1-ylmethyl-5-oxo-2-p-tolyl-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester
Synonyms: 8-cyclopropyl-7-naphthalen-1-ylmethyl-5-oxo-2-p-tolyl-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester
CAS NO:1235550-95-4
Molecular Formula:
Molecular Weight: 479.599
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: 8-cyclopropyl-7-naphthalen-1-ylmethyl-5-oxo-2-p-tolyl-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 8-cyclopropyl-7-naphthalen-1-ylmethyl-5-oxo-2-p-tolyl-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester(1235550-95-4)
EPA Substance Registry System: 8-cyclopropyl-7-naphthalen-1-ylmethyl-5-oxo-2-p-tolyl-5H-thiazolo[3,2-a]pyridine-3-carboxylic acid methyl ester(1235550-95-4)

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: 1235550-95-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1235550-95-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,5,5 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1235550-95:
(9*1)+(8*2)+(7*3)+(6*5)+(5*5)+(4*5)+(3*0)+(2*9)+(1*5)=144
144 % 10 = 4
So 1235550-95-4 is a valid CAS Registry Number.

1235550-95-4Upstream product

5720-05-8 4-methylphenylboronic acid

1235550-95-4Downstream Products

1235551-09-3 5-cyclopropyl-4-[(1-naphthyl)methyl]-2-oxo-8-(p-tolyl)-7-thia-1-azabicyclo[4.3.0]nona-3,5,8-triene-9-carboxylic acid

1235550-95-4Relevant academic research and scientific papers

Design and synthesis of C-2 substituted thiazolo and dihydrothiazolo ring-fused 2-pyridones: Pilicides with increased antivirulence activity

Chorell, Erik,Pinkner, Jerome S.,Phan, Gilles,Edvinsson, Sofie,Buelens, Floris,Remaut, Han,Waksman, Gabriel,Hultgren, Scott J.,Almqvist, Fredrik

supporting information; experimental part, p. 5690 - 5695 (2010/10/20)

Pilicides block pili formation by binding to pilus chaperones and blocking their function in the chaperone/usher pathway in E. coli. Various C-2 substituents were introduced on the pilicide scaffold by design and synthetic method developments. Experimenta

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