Cas 298181-29-0,(1R,2S,4R,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-3,3-dimethyl-5-phenylsulfanyl-cyclopentanecarbonitrile

298181-29-0

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Basic information

Product Name: (1R,2S,4R,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-3,3-dimethyl-5-phenylsulfanyl-cyclopentanecarbonitrile
Synonyms: (1R,2S,4R,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-3,3-dimethyl-5-phenylsulfanyl-cyclopentanecarbonitrile
CAS NO:298181-29-0
Molecular Formula:
Molecular Weight: 377.623
EINECS: N/A
Product Categories: N/A
Mol File: 298181-29-0.mol
Article Data: 1

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: (1R,2S,4R,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-3,3-dimethyl-5-phenylsulfanyl-cyclopentanecarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,4R,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-3,3-dimethyl-5-phenylsulfanyl-cyclopentanecarbonitrile(298181-29-0)
EPA Substance Registry System: (1R,2S,4R,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-3,3-dimethyl-5-phenylsulfanyl-cyclopentanecarbonitrile(298181-29-0)

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: 298181-29-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 298181-29-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,1,8 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 298181-29:
(8*2)+(7*9)+(6*8)+(5*1)+(4*8)+(3*1)+(2*2)+(1*9)=180
180 % 10 = 0
So 298181-29-0 is a valid CAS Registry Number.

298181-29-0Upstream product

298181-29-0Downstream Products

298181-33-6 C₂₃H₃₈O₄Si

298181-29-0Relevant articles and documents

New route to the synthesis of the illudane skeleton by Michael-Michael- elimination reaction

Tokuzaki, Kazuo,Kanemitu, Yasuhiro,Yoshimitsu, Takehiko,Nagaoka, Hiroto

, p. 5923 - 5926 (2007/10/03)

A new route to the synthesis of an optically active illudane skeleton from (R)-(-)-pantolactone (4) is established. The tricyclic ring system was constructed by Michael-Michael-elimination reaction of the enolate of (3S,5R)-3-(tert-butyldimethylsilyloxy)-

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