Cas 949007-15-2,(+)-N-[(1S,2S,3R)-4,4,4-trichloro-3-hydroxy-2-methyl-1-phenylbutan-1-yl]-2-thiophenesulfonamide

949007-15-2

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Basic information

Product Name: (+)-N-[(1S,2S,3R)-4,4,4-trichloro-3-hydroxy-2-methyl-1-phenylbutan-1-yl]-2-thiophenesulfonamide
Synonyms: (+)-N-[(1S,2S,3R)-4,4,4-trichloro-3-hydroxy-2-methyl-1-phenylbutan-1-yl]-2-thiophenesulfonamide
CAS NO:949007-15-2
Molecular Formula:
Molecular Weight: 428.788
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: (+)-N-[(1S,2S,3R)-4,4,4-trichloro-3-hydroxy-2-methyl-1-phenylbutan-1-yl]-2-thiophenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (+)-N-[(1S,2S,3R)-4,4,4-trichloro-3-hydroxy-2-methyl-1-phenylbutan-1-yl]-2-thiophenesulfonamide(949007-15-2)
EPA Substance Registry System: (+)-N-[(1S,2S,3R)-4,4,4-trichloro-3-hydroxy-2-methyl-1-phenylbutan-1-yl]-2-thiophenesulfonamide(949007-15-2)

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: 949007-15-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 949007-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,0,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 949007-15:
(8*9)+(7*4)+(6*9)+(5*0)+(4*0)+(3*7)+(2*1)+(1*5)=182
182 % 10 = 2
So 949007-15-2 is a valid CAS Registry Number.

949007-15-2Upstream product

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949007-15-2Relevant academic research and scientific papers

Lanthanum aryloxide/pybox-catalyzed direct asymmetric mannich-type reactions using a trichloromethyl ketone as a propionate equivalent donor

Morimoto, Hiroyuki,Lu, Gang,Aoyama, Naohiro,Matsunaga, Shigeki,Shibasaki, Masakatsu

, p. 9588 - 9589 (2008/02/13)

Direct catalytic asymmetric Mannich-type reaction of a trichloromethyl ketone as a propionate equivalent donor is described. A new lanthanum aryloxide-iPr-pybox + lithium aryloxide combined catalyst was the most effective, promoting the reaction of N-2-th

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