Cas 924310-88-3,2H-1,4-Benzoxazin-3(4H)-one, 4-[2-[(1,1-dimethylethyl)amino]-3-benzofuranyl]-7-methyl-

924310-88-3

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Basic information

Product Name: 2H-1,4-Benzoxazin-3(4H)-one, 4-[2-[(1,1-dimethylethyl)amino]-3-benzofuranyl]-7-methyl-
Synonyms: 2H-1,4-Benzoxazin-3(4H)-one, 4-[2-[(1,1-dimethylethyl)amino]-3-benzofuranyl]-7-methyl-
CAS NO:924310-88-3
Molecular Formula: C21H22N2O3
Molecular Weight: 0
EINECS: N/A
Product Categories: N/A
Mol File: 924310-88-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2H-1,4-Benzoxazin-3(4H)-one, 4-[2-[(1,1-dimethylethyl)amino]-3-benzofuranyl]-7-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2H-1,4-Benzoxazin-3(4H)-one, 4-[2-[(1,1-dimethylethyl)amino]-3-benzofuranyl]-7-methyl-(924310-88-3)
EPA Substance Registry System: 2H-1,4-Benzoxazin-3(4H)-one, 4-[2-[(1,1-dimethylethyl)amino]-3-benzofuranyl]-7-methyl-(924310-88-3)

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: 924310-88-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 924310-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,3,1 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 924310-88:
(8*9)+(7*2)+(6*4)+(5*3)+(4*1)+(3*0)+(2*8)+(1*8)=153
153 % 10 = 3
So 924310-88-3 is a valid CAS Registry Number.

924310-88-3Upstream product

924310-88-3Downstream Products

924310-88-3Relevant academic research and scientific papers

Isolation and characterization of 2-alkylaminobenzo[b]furans. Evidence for competing O-arylation in Cu-catalyzed intramolecular amidation

Feng, Gaofeng,Wu, Jinlong,Dai, Wei-Min

, p. 401 - 404 (2007)

2-Alkylaminobenzo[b]furans were isolated and characterized by X-ray crystal structural analysis, for the first time, from the Cu-catalyzed intramolecular amidation of hindered secondary amides under controlled microwave heating. A mechanism was proposed t

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