CAS: 66835-10-7 C10 H17 N O MW: 167.25169000

Identification

Namemyrtine
CAS Number66835-10-7
FDA UNIISearch
Molecular FormulaC10 H17 N O
Molecular Weight167.25169000
Nikkaji NumberJ19.966D

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 8.109e+004 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for myrtine usage levels up tonot for fragrance use.
Recommendation for myrtine flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

Vaccinium myrtillus shoot

Synonyms

(4R,9aR)-4- methyl-1,3,4,6,7,8,9,9a-octahydroquinolizin-2-one PubMed: Polymer-supported (-)-8-phenylmenthyl Auxiliary as an Effective Solidphase Chiral Inductor in the Addition of Nucleophiles to N-acyliminium Ions. PubMed: Electrochemical access to 8-(1-phenyl-ethyl)-1,4-dioxa-8-aza-spiro[4.5]decane-7-carbonitrile. Application to the asymmetric syntheses of (+)-myrtine and alkaloid (+)-241D. PubMed: Stereoselective synthesis of 2,6-cis- and 2,6-trans-piperidines through organocatalytic aza-Michael reactions: a facile synthesis of (+)-myrtine and (-)-epimyrtine. PubMed: Catalytic asymmetric synthesis of the alkaloid (+)-myrtine. PubMed: A convenient allylsilane-N-acyliminium route toward indolizidine and quinolizidine alkaloids. PubMed: Asymmetric synthesis of ring functionalized trans-2,6-disubstituted piperidines from N-sulfinyl delta-amino beta-keto phosphonates. total synthesis of (-)-myrtine. PubMed: Indolizidine and quinolizidine alkaloids. PubMed: Synthesis of the quinolizidine alkaloids (-)-lasubine II and (+/-)-myrtine by conjugate addition and intramolecular acylation of amino esters with acetylenic sulfones.