Cas 1322089-56-4,9,9-difluoro-9a-phenyl-2,3,9,9a-tetrahydrooxazolo[3,2-a]indole

1322089-56-4

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Basic information

Product Name: 9,9-difluoro-9a-phenyl-2,3,9,9a-tetrahydrooxazolo[3,2-a]indole
Synonyms: 9,9-difluoro-9a-phenyl-2,3,9,9a-tetrahydrooxazolo[3,2-a]indole
CAS NO:1322089-56-4
Molecular Formula:
Molecular Weight: 273.282
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: 9,9-difluoro-9a-phenyl-2,3,9,9a-tetrahydrooxazolo[3,2-a]indole(CAS DataBase Reference)
NIST Chemistry Reference: 9,9-difluoro-9a-phenyl-2,3,9,9a-tetrahydrooxazolo[3,2-a]indole(1322089-56-4)
EPA Substance Registry System: 9,9-difluoro-9a-phenyl-2,3,9,9a-tetrahydrooxazolo[3,2-a]indole(1322089-56-4)

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: 1322089-56-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1322089-56-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,2,0,8 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1322089-56:
(9*1)+(8*3)+(7*2)+(6*2)+(5*0)+(4*8)+(3*9)+(2*5)+(1*6)=134
134 % 10 = 4
So 1322089-56-4 is a valid CAS Registry Number.

1322089-56-4Upstream product

139600-93-4 2-(2-phenyl-1H-indol-1-yl)ethan-1-ol

1322089-56-4Downstream Products

1322089-56-4Relevant academic research and scientific papers

An efficient difluorohydroxylation of indoles using selectfluor as a fluorinating reagent

Lin, Riyuan,Ding, Shengtao,Shi, Zhuangzhi,Jiao, Ning

supporting information; experimental part, p. 4498 - 4501 (2011/10/12)

An efficient difluorohydroxylation of substituted indoles leading to 3,3-difluoroindolin-2-ols with good yields by using Selectfluor as the electrophilic fluorinating reagent has been developed. In this methodology, the indole rings were difluorinated hig

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