Cas 1262285-95-9,tert-butyl 1-((R)-((S)-1,1-dimethylethyl-sulfinamido)(phenyl)methyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate

1262285-95-9

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Basic information

Product Name: tert-butyl 1-((R)-((S)-1,1-dimethylethyl-sulfinamido)(phenyl)methyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate
Synonyms: tert-butyl 1-((R)-((S)-1,1-dimethylethyl-sulfinamido)(phenyl)methyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate
CAS NO:1262285-95-9
Molecular Formula:
Molecular Weight: 406.59
EINECS: N/A
Product Categories: N/A
Mol File: 1262285-95-9.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: tert-butyl 1-((R)-((S)-1,1-dimethylethyl-sulfinamido)(phenyl)methyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 1-((R)-((S)-1,1-dimethylethyl-sulfinamido)(phenyl)methyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate(1262285-95-9)
EPA Substance Registry System: tert-butyl 1-((R)-((S)-1,1-dimethylethyl-sulfinamido)(phenyl)methyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate(1262285-95-9)

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: 1262285-95-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262285-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,2,8 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1262285-95:
(9*1)+(8*2)+(7*6)+(6*2)+(5*2)+(4*8)+(3*5)+(2*9)+(1*5)=159
159 % 10 = 9
So 1262285-95-9 is a valid CAS Registry Number.

1262285-95-9Upstream product

1262285-95-9Downstream Products

1262285-93-7 tert-butyl (R)-1-[amino(phenyl)methyl]-7-azabicyclo[2.2.1]heptane-7-carboxylate

1262285-95-9Relevant articles and documents

Efficient synthesis of a 7-azabicyclo[2.2.1]heptane based GlyT1 uptake inhibitor

Xiong, Hui,Frietze, William,Andisik, Donald W.,Ernst, Glen E.,Palmer, William E.,Hinkley, Lindsay,Varnes, Jeffrey G.,Albert, Jeffrey S.,Veale, Chris A.

experimental part, p. 6741 - 6744 (2011/02/25)

An efficient synthetic route based on generation and subsequent electrophilic reaction of a Boc-protected azabicyclo[2.2.1]heptane anion to prepare a potent GlyT1 uptake inhibitor (1) is described.

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