Cas 1241391-08-1,6,6,6-trichloro-5-hydroxy-1-phenyl-2-(p-tosylamino)hexan-3-one

1241391-08-1

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Basic information

Product Name: 6,6,6-trichloro-5-hydroxy-1-phenyl-2-(p-tosylamino)hexan-3-one
Synonyms: 6,6,6-trichloro-5-hydroxy-1-phenyl-2-(p-tosylamino)hexan-3-one
CAS NO:1241391-08-1
Molecular Formula:
Molecular Weight: 464.797
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: 6,6,6-trichloro-5-hydroxy-1-phenyl-2-(p-tosylamino)hexan-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 6,6,6-trichloro-5-hydroxy-1-phenyl-2-(p-tosylamino)hexan-3-one(1241391-08-1)
EPA Substance Registry System: 6,6,6-trichloro-5-hydroxy-1-phenyl-2-(p-tosylamino)hexan-3-one(1241391-08-1)

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: 1241391-08-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1241391-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,3,9 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1241391-08:
(9*1)+(8*2)+(7*4)+(6*1)+(5*3)+(4*9)+(3*1)+(2*0)+(1*8)=121
121 % 10 = 1
So 1241391-08-1 is a valid CAS Registry Number.

1241391-08-1Upstream product

75-87-6 chloral

1241391-08-1Downstream Products

1241391-08-1Relevant academic research and scientific papers

Reductive aldol and mannich-type reactions of azetidin-3-ones promoted by titanium tetraiodide

Hata, Shingo,Fukuda, Daisuke,Hachiya, Iwao,Shimizu, Makoto

supporting information; experimental part, p. 473 - 477 (2010/08/23)

A convenient method is described for the generation and reaction of the enolates of aminoacetone equivalents, which uses the reduction of azetidin-3-one with titanium tetraiodide and subsequent reactions with electrophiles. This methodology provides a str

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