Cas 1142812-06-3,(4S,5R)-N-(2-(1H-imidazol-4-yl)ethyl)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carboxamide

1142812-06-3

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Basic information

Product Name: (4S,5R)-N-(2-(1H-imidazol-4-yl)ethyl)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carboxamide
Synonyms: (4S,5R)-N-(2-(1H-imidazol-4-yl)ethyl)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carboxamide
CAS NO:1142812-06-3
Molecular Formula:
Molecular Weight: 330.343
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: (4S,5R)-N-(2-(1H-imidazol-4-yl)ethyl)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-N-(2-(1H-imidazol-4-yl)ethyl)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carboxamide(1142812-06-3)
EPA Substance Registry System: (4S,5R)-N-(2-(1H-imidazol-4-yl)ethyl)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carboxamide(1142812-06-3)

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: 1142812-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1142812-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,2,8,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1142812-06:
(9*1)+(8*1)+(7*4)+(6*2)+(5*8)+(4*1)+(3*2)+(2*0)+(1*6)=113
113 % 10 = 3
So 1142812-06-3 is a valid CAS Registry Number.

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1142812-06-3Relevant academic research and scientific papers

Key Structural Elements for Cellular Uptake of Acinetobactin, a Major Siderophore of Acinetobacter baumannii

Song, Woon Young,Jeong, Dawa,Kim, Jimin,Lee, Min Wook,Oh, Man Hwan,Kim, Hak Joong

, p. 500 - 503 (2017)

Acinetobactin is a major siderophore utilized by the human pathogen Acinetobacter baumannii. The rapid acquisition of drug resistance by A. baumannii has garnered concern globally. Herein, acinetobactin and systematically generated analogues were prepared

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