Cas 1108200-15-2,(2S,3S)-N-acetyl-1-chloro-1,1-difluoro-3-methyl-3-phenyl-2-propyl amine

1108200-15-2

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Basic information

Product Name: (2S,3S)-N-acetyl-1-chloro-1,1-difluoro-3-methyl-3-phenyl-2-propyl amine
Synonyms: (2S,3S)-N-acetyl-1-chloro-1,1-difluoro-3-methyl-3-phenyl-2-propyl amine
CAS NO:1108200-15-2
Molecular Formula:
Molecular Weight: 261.699
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: (2S,3S)-N-acetyl-1-chloro-1,1-difluoro-3-methyl-3-phenyl-2-propyl amine(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-N-acetyl-1-chloro-1,1-difluoro-3-methyl-3-phenyl-2-propyl amine(1108200-15-2)
EPA Substance Registry System: (2S,3S)-N-acetyl-1-chloro-1,1-difluoro-3-methyl-3-phenyl-2-propyl amine(1108200-15-2)

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: 1108200-15-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1108200-15-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,8,2,0 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1108200-15:
(9*1)+(8*1)+(7*0)+(6*8)+(5*2)+(4*0)+(3*0)+(2*1)+(1*5)=82
82 % 10 = 2
So 1108200-15-2 is a valid CAS Registry Number.

1108200-15-2Upstream product

108-24-7 acetic anhydride

1108200-15-2Downstream Products

1108200-15-2Relevant academic research and scientific papers

A new strategy for the synthesis of optically pure β-fluoroalkyl β-amino acid derivatives

Fustero, Santos,Pozo, Carlos Del,Catalan, Silvia,Aleman, Jose,Parra, Alejandro,Marcos, Vanesa,Ruano, Jose Luis Garcia

, p. 641 - 644 (2009)

(Chemical Equation Presented) The first general approach for the diastereoselective formation of a variety of optically pure anti/β- fluoroalkyl β-amino acid derivatives is described. The process relies on the stereocontrolled reaction, mediated by a remo

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