Cas 193401-77-3,6-(2-benzyloxy)ethyl-7-nitro-2,3-dihydropyrrolo[1,2,3-d,e]benzoxazine

193401-77-3

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Basic information

Product Name: 6-(2-benzyloxy)ethyl-7-nitro-2,3-dihydropyrrolo[1,2,3-d,e]benzoxazine
Synonyms: 6-(2-benzyloxy)ethyl-7-nitro-2,3-dihydropyrrolo[1,2,3-d,e]benzoxazine
CAS NO:193401-77-3
Molecular Formula:
Molecular Weight: 338.363
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: 6-(2-benzyloxy)ethyl-7-nitro-2,3-dihydropyrrolo[1,2,3-d,e]benzoxazine(CAS DataBase Reference)
NIST Chemistry Reference: 6-(2-benzyloxy)ethyl-7-nitro-2,3-dihydropyrrolo[1,2,3-d,e]benzoxazine(193401-77-3)
EPA Substance Registry System: 6-(2-benzyloxy)ethyl-7-nitro-2,3-dihydropyrrolo[1,2,3-d,e]benzoxazine(193401-77-3)

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: 193401-77-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 193401-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 193401-77:
(8*1)+(7*9)+(6*3)+(5*4)+(4*0)+(3*1)+(2*7)+(1*7)=133
133 % 10 = 3
So 193401-77-3 is a valid CAS Registry Number.

193401-77-3Upstream product

193401-76-2 4-benzyloxybutanal, 4-amino-2,3-dihydro-6-nitro-1,4-benzoxazine hydrazone

193401-77-3Downstream Products

193401-77-3Relevant academic research and scientific papers

A novel method for suppression of the abnormal Fischer indole synthesis

Szczepankiewicz, Bruce G.,Heathcock, Clayton H.

, p. 8853 - 8870 (1997)

A method is described for the use of the Fischer indole synthesis to prepare 7-hydroxy-indoles in good yield. The method involves the construction of a 4-aminobenzoxazine and removal of the N-O tether after the indole has been formed.

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