Cas 770743-74-3,(S<sub>S</sub>,S)-(+)-N-(p-toluenesulfinyl)-2-(1-amino-2-methylpropyl)-2-methyl-1,3-dithiane

770743-74-3

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Basic information

Product Name: (S_S,S)-(+)-N-(p-toluenesulfinyl)-2-(1-amino-2-methylpropyl)-2-methyl-1,3-dithiane
Synonyms: (S_S,S)-(+)-N-(p-toluenesulfinyl)-2-(1-amino-2-methylpropyl)-2-methyl-1,3-dithiane
CAS NO:770743-74-3
Molecular Formula:
Molecular Weight: 343.579
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: (S_S,S)-(+)-N-(p-toluenesulfinyl)-2-(1-amino-2-methylpropyl)-2-methyl-1,3-dithiane(CAS DataBase Reference)
NIST Chemistry Reference: (S_S,S)-(+)-N-(p-toluenesulfinyl)-2-(1-amino-2-methylpropyl)-2-methyl-1,3-dithiane(770743-74-3)
EPA Substance Registry System: (S_S,S)-(+)-N-(p-toluenesulfinyl)-2-(1-amino-2-methylpropyl)-2-methyl-1,3-dithiane(770743-74-3)

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: 770743-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 770743-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,0,7,4 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 770743-74:
(8*7)+(7*7)+(6*0)+(5*7)+(4*4)+(3*3)+(2*7)+(1*4)=183
183 % 10 = 3
So 770743-74-3 is a valid CAS Registry Number.

770743-74-3Upstream product

770743-74-3Downstream Products

770743-74-3Relevant academic research and scientific papers

Asymmetric synthesis of α-amino 1,3-dithioketals from sulfinimines (N-sulfinyl imines). Synthesis of (2S,3R)-(-)-3-hydroxy-3-methylproline

Davis, Franklin A.,Ramachandar, Tokala,Liu, Hu

, p. 3393 - 3395 (2004)

(Chemical Equation Presented) N-Sulfinyl α-amino 1,3-dithioketals are prepared in high de and good yield by treating sulfinimines with lithio-1,3-dithianes. Selective removal of the N-sulfinyl or the thioketal groups affords stable α-amino 1,3-dithioketal

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