Cas 665054-35-3,7-Oxabicyclo[2.2.1]heptane-2-carboxylicacid,3-amino-,(1R,2R,3R,4S)-rel-(9CI)

665054-35-3

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Basic information

Product Name: 7-Oxabicyclo[2.2.1]heptane-2-carboxylicacid,3-amino-,(1R,2R,3R,4S)-rel-(9CI)
Synonyms: 7-Oxabicyclo[2.2.1]heptane-2-carboxylicacid,3-amino-,(1R,2R,3R,4S)-rel-(9CI)
CAS NO:665054-35-3
Molecular Formula: C7H11NO3
Molecular Weight: 157.16714
EINECS: N/A
Product Categories: CARBOXYLICACID
Mol File: 665054-35-3.mol

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: 7-Oxabicyclo[2.2.1]heptane-2-carboxylicacid,3-amino-,(1R,2R,3R,4S)-rel-(9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 7-Oxabicyclo[2.2.1]heptane-2-carboxylicacid,3-amino-,(1R,2R,3R,4S)-rel-(9CI)(665054-35-3)
EPA Substance Registry System: 7-Oxabicyclo[2.2.1]heptane-2-carboxylicacid,3-amino-,(1R,2R,3R,4S)-rel-(9CI)(665054-35-3)

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: 665054-35-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 665054-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,5,0,5 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 665054-35:
(8*6)+(7*6)+(6*5)+(5*0)+(4*5)+(3*4)+(2*3)+(1*5)=163
163 % 10 = 3
So 665054-35-3 is a valid CAS Registry Number.

665054-35-3Upstream product

112918-09-9 methyl 3-exo-(benzyloxycarbonylamino)-7-oxabicyclo<2.2.1>heptane-2-exo-carboxylate

665054-35-3Downstream Products

665054-35-3Relevant academic research and scientific papers

U-4C-3CR versus U-5C-4CR and stereochemical outcomes using suitable bicyclic β-amino acid derivatives as bifunctional components in the Ugi reaction

Basso, Andrea,Banfi, Luca,Riva, Renata,Guanti, Giuseppe

, p. 587 - 590 (2004)

Intramolecular Ugi reactions with bicyclic β-amino acids have been performed and the effects of the configuration and N-alkylation have been studied. We have proven that preferential ring contraction or nucleophilic attack by the solvent depend not only o

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