Cas 1312297-21-4,4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one

1312297-21-4

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Basic information

Product Name: 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one
Synonyms: 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one
CAS NO:1312297-21-4
Molecular Formula:
Molecular Weight: 312.282
EINECS: N/A
Product Categories: N/A
Mol File: 1312297-21-4.mol
Article Data: 1

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: 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one(1312297-21-4)
EPA Substance Registry System: 4-((2-hydroxy-5-methoxyphenyl)(hydroxyimino)methyl)-1H-benzo[d][1,2]oxazin-1-one(1312297-21-4)

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: 1312297-21-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312297-21-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,2,9 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1312297-21:
(9*1)+(8*3)+(7*1)+(6*2)+(5*2)+(4*9)+(3*7)+(2*2)+(1*1)=124
124 % 10 = 4
So 1312297-21-4 is a valid CAS Registry Number.

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1312297-21-4Relevant articles and documents

A simple synthesis of 4-substituted 2,3-benzoxazinones from C-2 arylated 1,3-indanediones

Das, Suven,Koley, Pradyot,Pramanik, Animesh

experimental part, p. 3243 - 3246 (2011/06/28)

A simple one-pot procedure for the conversion of 2-hydroxy-2-(2′- hydroxy-aryl)-1,3-indanediones to 4-substituted benzoxazinones has been developed. The process constitutes an interesting acid-catalyzed rearrangement followed by condensation with hydroxyl

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