Cas 171010-53-0,5-Methoxy-2-methyl-pyrimidine-4-carboxylic acid (6-carbamoyl-2-hydroxy-3-methyl-phenyl)-amide

171010-53-0

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Basic information

Product Name: 5-Methoxy-2-methyl-pyrimidine-4-carboxylic acid (6-carbamoyl-2-hydroxy-3-methyl-phenyl)-amide
Synonyms: 5-Methoxy-2-methyl-pyrimidine-4-carboxylic acid (6-carbamoyl-2-hydroxy-3-methyl-phenyl)-amide
CAS NO:171010-53-0
Molecular Formula:
Molecular Weight: 316.316
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: 5-Methoxy-2-methyl-pyrimidine-4-carboxylic acid (6-carbamoyl-2-hydroxy-3-methyl-phenyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 5-Methoxy-2-methyl-pyrimidine-4-carboxylic acid (6-carbamoyl-2-hydroxy-3-methyl-phenyl)-amide(171010-53-0)
EPA Substance Registry System: 5-Methoxy-2-methyl-pyrimidine-4-carboxylic acid (6-carbamoyl-2-hydroxy-3-methyl-phenyl)-amide(171010-53-0)

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: 171010-53-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 171010-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,1 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 171010-53:
(8*1)+(7*7)+(6*1)+(5*0)+(4*1)+(3*0)+(2*5)+(1*3)=80
80 % 10 = 0
So 171010-53-0 is a valid CAS Registry Number.

171010-53-0Upstream product

113949-10-3 5-methoxy-2-methylpyrimidine-4-carboxylic acid

171010-53-0Downstream Products

171010-53-0Relevant academic research and scientific papers

Synthesis of Boxazomycin B and Related Analogs

Suto, Mark J.,Turner, William R.

, p. 7213 - 7216 (1995)

The total synthesis of the novel antibacterial agent Boxazomycin B is reported.The synthesis proceeds through a highly functionalized benzene ring in which the key functionalities are introduced early in the synthesis and serve as protecting groups for ad

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