Cas 1574475-21-0,(R)-N-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide

1574475-21-0

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Basic information

Product Name: (R)-N-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide
Synonyms: (R)-N-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide
CAS NO:1574475-21-0
Molecular Formula:
Molecular Weight: 357.517
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-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide(1574475-21-0)
EPA Substance Registry System: (R)-N-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide(1574475-21-0)

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: 1574475-21-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1574475-21-0 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 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1574475-21:
(9*1)+(8*5)+(7*7)+(6*4)+(5*4)+(4*7)+(3*5)+(2*2)+(1*1)=190
190 % 10 = 0
So 1574475-21-0 is a valid CAS Registry Number.

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1574475-21-0Relevant 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

supporting information, 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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