Cas 877776-33-5,(R)-2,2,2-Trifluoro-1-[1-((R)-2,4,6-triisopropyl-benzenesulfinyl)-naphthalen-2-yl]-ethanol

877776-33-5

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Basic information

Product Name: (R)-2,2,2-Trifluoro-1-[1-((R)-2,4,6-triisopropyl-benzenesulfinyl)-naphthalen-2-yl]-ethanol
Synonyms:
CAS NO:877776-33-5
Molecular Formula:
Molecular Weight: 476.603
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: (R)-2,2,2-Trifluoro-1-[1-((R)-2,4,6-triisopropyl-benzenesulfinyl)-naphthalen-2-yl]-ethanol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2,2,2-Trifluoro-1-[1-((R)-2,4,6-triisopropyl-benzenesulfinyl)-naphthalen-2-yl]-ethanol(877776-33-5)
EPA Substance Registry System: (R)-2,2,2-Trifluoro-1-[1-((R)-2,4,6-triisopropyl-benzenesulfinyl)-naphthalen-2-yl]-ethanol(877776-33-5)

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: 877776-33-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 877776-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,7,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 877776-33:
(8*8)+(7*7)+(6*7)+(5*7)+(4*7)+(3*6)+(2*3)+(1*3)=245
245 % 10 = 5
So 877776-33-5 is a valid CAS Registry Number.

877776-33-5Upstream product

289473-20-7 (R_S)-1-[(2,4,6-triisopropyl)sulfinyl]-2-naphthaldehyde

877776-33-5Downstream Products

877776-33-5Relevant academic research and scientific papers

Remote asymmetric trifluoromethylation induced by chiral sulfinyl group: Synthesis of enantiomerically pure 1-(2-naphthyl)-2,2,2-trifluoroethanol

Sugimoto, Hideki,Nakamura, Shuichi,Shibata, Yoshihiro,Shibata, Norio,Toru, Takeshi

, p. 1337 - 1340 (2006)

The reaction of 1-[(2,4,6-triisopropylphenyl)sulfinyl]-2-naphthaldehyde with (trifluoromethyl)trimethylsilane using tetramethylammonium fluoride gave trifluoromethylated compounds in high yield with high diastereoselectivity. Desilylation and subsequent r

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