Cas 1071701-84-2,(1R)-3A,6A-DIMETHYLHEXAHYDRO-1,4-METHANOCYCLOPENTA[C]PYRROLE-1(2H)-CARBOXYLIC ACID

1071701-84-2

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Basic information

Product Name: (1R)-3A,6A-DIMETHYLHEXAHYDRO-1,4-METHANOCYCLOPENTA[C]PYRROLE-1(2H)-CARBOXYLIC ACID
Synonyms: (1R)-3A,6A-DIMETHYLHEXAHYDRO-1,4-METHANOCYCLOPENTA[C]PYRROLE-1(2H)-CARBOXYLIC ACID
CAS NO:1071701-84-2
Molecular Formula: C11H17NO2
Molecular Weight: 195.25818
EINECS: N/A
Product Categories: N/A
Mol File: 1071701-84-2.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1R)-3A,6A-DIMETHYLHEXAHYDRO-1,4-METHANOCYCLOPENTA[C]PYRROLE-1(2H)-CARBOXYLIC ACID(CAS DataBase Reference)
NIST Chemistry Reference: (1R)-3A,6A-DIMETHYLHEXAHYDRO-1,4-METHANOCYCLOPENTA[C]PYRROLE-1(2H)-CARBOXYLIC ACID(1071701-84-2)
EPA Substance Registry System: (1R)-3A,6A-DIMETHYLHEXAHYDRO-1,4-METHANOCYCLOPENTA[C]PYRROLE-1(2H)-CARBOXYLIC ACID(1071701-84-2)

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: 1071701-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1071701-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,7,0 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1071701-84:
(9*1)+(8*0)+(7*7)+(6*1)+(5*7)+(4*0)+(3*1)+(2*8)+(1*4)=122
122 % 10 = 2
So 1071701-84-2 is a valid CAS Registry Number.

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1071701-84-2Relevant articles and documents

A chiral tricyclic proline analogue obtained from camphor

Gorichko, Marian V,Grygorenko, Oleksandr O,Komarov, Igor V

, p. 9411 - 9412 (2007/10/03)

Synthesis of 3a,6a-dimethylhexahydro-1,4-methanocyclopenta[c]pyrrole-1(2H)-carboxylic acid, a new chiral constrained proline analogue is reported. The synthesis was accomplished in five steps from 8-bromocamphor, easily available in both enantiomeric forms. A key step in the synthesis is an intramolecular 'domino'-type cyclisation, initiated by a nucleophile attack at an activated C=N bond.

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