Cas 1335302-46-9,(R)-N-((1R,2R)-1-([1,1'-biphenyl]-3-yl)-2-fluoro-3-phenylpropyl)-2-methylpropane-2-sulfinamide

1335302-46-9

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Basic information

Product Name: (R)-N-((1R,2R)-1-([1,1'-biphenyl]-3-yl)-2-fluoro-3-phenylpropyl)-2-methylpropane-2-sulfinamide
Synonyms: (R)-N-((1R,2R)-1-([1,1'-biphenyl]-3-yl)-2-fluoro-3-phenylpropyl)-2-methylpropane-2-sulfinamide
CAS NO:1335302-46-9
Molecular Formula:
Molecular Weight: 409.568
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-((1R,2R)-1-([1,1'-biphenyl]-3-yl)-2-fluoro-3-phenylpropyl)-2-methylpropane-2-sulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-((1R,2R)-1-([1,1'-biphenyl]-3-yl)-2-fluoro-3-phenylpropyl)-2-methylpropane-2-sulfinamide(1335302-46-9)
EPA Substance Registry System: (R)-N-((1R,2R)-1-([1,1'-biphenyl]-3-yl)-2-fluoro-3-phenylpropyl)-2-methylpropane-2-sulfinamide(1335302-46-9)

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: 1335302-46-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1335302-46-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,3,0 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1335302-46:
(9*1)+(8*3)+(7*3)+(6*5)+(5*3)+(4*0)+(3*2)+(2*4)+(1*6)=119
119 % 10 = 9
So 1335302-46-9 is a valid CAS Registry Number.

1335302-46-9Upstream product

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1335302-46-9Relevant academic research and scientific papers

Highly diastereoselective and general synthesis of primary β-fluoroamines

Schulte, Michael L.,Lindsley, Craig W.

supporting information; experimental part, p. 5684 - 5687 (2011/12/05)

A short, high yielding protocol has been developed for the highly diastereoselective (dr >20:1) and general synthesis of primary β-fluoroamines by the enantioselective α-fluorination of aldehydes, conversion into the N-sulfinyl aldimine, nucleophilic addi

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