Cas 1574474-96-6,(R)-N-((3R,4S)-3-hydroxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl)tert-butylsulfinamide

1574474-96-6

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Basic information

Product Name: (R)-N-((3R,4S)-3-hydroxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl)tert-butylsulfinamide
Synonyms: (R)-N-((3R,4S)-3-hydroxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl)tert-butylsulfinamide
CAS NO:1574474-96-6
Molecular Formula:
Molecular Weight: 345.463
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)-N-((3R,4S)-3-hydroxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl)tert-butylsulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-((3R,4S)-3-hydroxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl)tert-butylsulfinamide(1574474-96-6)
EPA Substance Registry System: (R)-N-((3R,4S)-3-hydroxy-3-phenyl-3,4-dihydro-2H-chromen-4-yl)tert-butylsulfinamide(1574474-96-6)

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: 1574474-96-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1574474-96-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,4,4,7 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1574474-96:
(9*1)+(8*5)+(7*7)+(6*4)+(5*4)+(4*7)+(3*4)+(2*9)+(1*6)=206
206 % 10 = 6
So 1574474-96-6 is a valid CAS Registry Number.

1574474-96-6Upstream product

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1574474-96-6Relevant academic research and scientific papers

Asymmetric synthesis of novel vicinal amino alcohols via intramolecular ketone- N -sulfinylimine pinacol-type reductive coupling promoted by SmI 2

Zhao, Yun-Hui,Liu, Han-Wen

, p. 1012 - 1018 (2014/03/21)

A novel intramolecular asymmetric ketone-N-sulfinylimine pinacol-type reductive coupling reaction induced by SmI2 was reported. A series of 1-amino-1,2,3,4-tetrahydronaphthalen-2-carbinols were obtained in moderate to good yields with excellent

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