Dehydroabietonitrile

Base Information

Chemical Name:Dehydroabietonitrile
CAS No.:31148-95-5
Molecular Formula:C20H27 N
Molecular Weight:281.441
Hs Code.:
European Community (EC) Number:250-488-6
NSC Number:146197,2954
DSSTox Substance ID:DTXSID40885494
Nikkaji Number:J278.056I
Wikidata:Q82864123
Mol file:31148-95-5.mol

Synonyms:Dehydroabietonitrile;Dehydroabietylnitrile;31148-95-5;1-Phenanthrenecarbonitrile, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aS,10aR)-;Podocarpa-8,13-triene-15-nitrile, 13-isopropyl-;1-Phenanthrenecarbonitrile,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1.alpha.,4a.beta.,10a.alpha.)]-;DTXSID40885494;NSC2954;1-Phenanthrenecarbonitrile, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1.alpha.,4a.beta.,10a.alpha.)]-;NSC-2954;NSC146197;NSC-146197

Suppliers and Price of Dehydroabietonitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 7 raw suppliers

Chemical Property of Dehydroabietonitrile

Chemical Property:

Boiling Point:402.4°Cat760mmHg
Flash Point:152.2°C
Density:1.01g/cm³
XLogP3:5.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:281.214349865
Heavy Atom Count:21
Complexity:444

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C#N)C
Isomeric SMILES:CC(C)C1=CC2=C(C=C1)[C@]3(CCC[C@@]([C@@H]3CC2)(C)C#N)C

Technology Process of Dehydroabietonitrile

There total 4 articles about Dehydroabietonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: 35928-32-6
(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxamide

: 31148-95-5
(+)-dehydroabietylnitrile

Guidance literature:: With tetrachloromethane; triethylamine; triphenylphosphine; In dichloromethane; for 17h; Inert atmosphere; Reflux;
DOI:10.1039/d1ra03546k

Reference yield: 88.0%

: 1446-61-3,104530-67-8,1416-08-6,24564-18-9,27174-94-3,66989-22-8,87926-74-7,25512-83-8
leelamine

: 31148-95-5
(+)-dehydroabietylnitrile

Guidance literature:: With pyridine; Oxone; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; Pyridine hydrobromide; In dichloromethane; at 20 ℃; for 12h; Green chemistry;
DOI:10.1002/chem.201600549