Cas 1219799-83-3,(R)-3-(N-((S)-1-azido-3-phenylpropan-2-yl)-4-methylphenylsulfonamido)-2-(tert-butoxycarbonylamino)propyl 4-methylbenzenesulfonate

1219799-83-3

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Basic information

Product Name: (R)-3-(N-((S)-1-azido-3-phenylpropan-2-yl)-4-methylphenylsulfonamido)-2-(tert-butoxycarbonylamino)propyl 4-methylbenzenesulfonate
Synonyms: (R)-3-(N-((S)-1-azido-3-phenylpropan-2-yl)-4-methylphenylsulfonamido)-2-(tert-butoxycarbonylamino)propyl 4-methylbenzenesulfonate
CAS NO:1219799-83-3
Molecular Formula:
Molecular Weight: 657.812
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)-3-(N-((S)-1-azido-3-phenylpropan-2-yl)-4-methylphenylsulfonamido)-2-(tert-butoxycarbonylamino)propyl 4-methylbenzenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-(N-((S)-1-azido-3-phenylpropan-2-yl)-4-methylphenylsulfonamido)-2-(tert-butoxycarbonylamino)propyl 4-methylbenzenesulfonate(1219799-83-3)
EPA Substance Registry System: (R)-3-(N-((S)-1-azido-3-phenylpropan-2-yl)-4-methylphenylsulfonamido)-2-(tert-butoxycarbonylamino)propyl 4-methylbenzenesulfonate(1219799-83-3)

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: 1219799-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1219799-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,7,9 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1219799-83:
(9*1)+(8*2)+(7*1)+(6*9)+(5*7)+(4*9)+(3*9)+(2*8)+(1*3)=203
203 % 10 = 3
So 1219799-83-3 is a valid CAS Registry Number.

1219799-83-3Upstream product

1219799-83-3Downstream Products

1219799-48-0 tert-butyl (2S,6S)-2-benzyl-1-tosyl-1,4-diazepan-6-ylcarbamate

1219799-83-3Relevant academic research and scientific papers

A new route to 1,4-oxazepanes and 1,4-diazepanes from Garner aldehyde

Das, Sanjit Kumar,Srivastava, Ajay Kumar,Panda, Gautam

supporting information; experimental part, p. 1483 - 1485 (2010/05/18)

A highly efficient and convenient method for the synthesis of substituted chiral 1,4-oxazepanes and 1,4-diazepanes have been described from Garner aldehyde through reductive amination with amino ester hydrochlorides followed by intramolecular cyclization as the key steps.

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