Cas 1582802-94-5,(S)-N-((R)-1-(2,6-dibromophenyl)-3-fluorobut-3-enyl)-2-methylpropane-2-sulfinamide

1582802-94-5

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Basic information

Product Name: (S)-N-((R)-1-(2,6-dibromophenyl)-3-fluorobut-3-enyl)-2-methylpropane-2-sulfinamide
Synonyms: (S)-N-((R)-1-(2,6-dibromophenyl)-3-fluorobut-3-enyl)-2-methylpropane-2-sulfinamide
CAS NO:1582802-94-5
Molecular Formula:
Molecular Weight: 427.175
EINECS: N/A
Product Categories: N/A
Mol File: 1582802-94-5.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: (S)-N-((R)-1-(2,6-dibromophenyl)-3-fluorobut-3-enyl)-2-methylpropane-2-sulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-((R)-1-(2,6-dibromophenyl)-3-fluorobut-3-enyl)-2-methylpropane-2-sulfinamide(1582802-94-5)
EPA Substance Registry System: (S)-N-((R)-1-(2,6-dibromophenyl)-3-fluorobut-3-enyl)-2-methylpropane-2-sulfinamide(1582802-94-5)

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: 1582802-94-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1582802-94-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,2,8,0 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1582802-94:
(9*1)+(8*5)+(7*8)+(6*2)+(5*8)+(4*0)+(3*2)+(2*9)+(1*4)=185
185 % 10 = 5
So 1582802-94-5 is a valid CAS Registry Number.

1582802-94-5Upstream product

6186-91-0 3-chloro-2-fluoropropene

1582802-94-5Downstream Products

1582802-94-5Relevant articles and documents

Indium-promoted diastereoselective addition of fluorinated haloallylic derivatives to imines

Lemonnier, Gérald,Hijfte, Nathalie Van,Poisson, Thomas,Couve-Bonnaire, Samuel,Pannecoucke, Xavier

, p. 2916 - 2925 (2014/05/06)

We report herein the first general access to fluorinated homoallylic amines by means of an addition of fluorinated organoindium reagent. The corresponding amines were obtained in good to excellent yield with excellent diastereoisomeric ratio. A plausible mechanism is proposed to explain the stereochemical outcome of the reaction based on the X-ray structure of the products.

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