Cas 86970-49-2,(5-Amino-2-oxo-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl)-carbamic acid ethyl ester

86970-49-2

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Basic information

Product Name: (5-Amino-2-oxo-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl)-carbamic acid ethyl ester
Synonyms:
CAS NO:86970-49-2
Molecular Formula:
Molecular Weight: 326.312
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-Amino-2-oxo-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl)-carbamic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5-Amino-2-oxo-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl)-carbamic acid ethyl ester(86970-49-2)
EPA Substance Registry System: (5-Amino-2-oxo-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl)-carbamic acid ethyl ester(86970-49-2)

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: 86970-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86970-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86970-49:
(7*8)+(6*6)+(5*9)+(4*7)+(3*0)+(2*4)+(1*9)=182
182 % 10 = 2
So 86970-49-2 is a valid CAS Registry Number.

86970-49-2Upstream product

15206-55-0 methyl 2-oxo-2-phenylacetate

86970-49-2Downstream Products

86970-49-2Relevant academic research and scientific papers

Synthesis of potential anticancer agents. Pyrido[4,3-b][1,4]oxazines and pyrido[4,3-b][1,4]thiazines

Temple, Carroll,Wheeler, Glynn P.,Comber, Robert N.,Elliott, Robert D.,Montgomery, John A.

, p. 1614 - 1619 (1983)

Hydrolysis of the chloro group of ethyl (6-amino-4-chloro-5-nitropyridin-2-yl)carbamate (3) with formic acid gave the corresponding 4-hydroxypyridine 4. Catalytic hydrogenation of the nitro group of 4 gave the 5-amino-4-hydroxypyridine 5, which was reacte

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