(1S,2S,5R)-Neomenthyl cyanide

Base Information Edit

Chemical Name:(1S,2S,5R)-Neomenthyl cyanide
CAS No.:180978-26-1
Molecular Formula:C11H19 N
Molecular Weight:165.279
Hs Code.:
DSSTox Substance ID:DTXSID20454187
Nikkaji Number:J1.677.960A
Wikidata:Q82275556
Mol file:180978-26-1.mol

Synonyms:(1S,2S,5R)-Neomenthyl cyanide;180978-26-1;(1S,2S,5R)-5-methyl-2-propan-2-ylcyclohexane-1-carbonitrile;Cyclohexanecarbonitrile, 5-methyl-2-(1-methylethyl)-, (1S,2S,5R)-;(1S,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexane-1-carbonitrile;SCHEMBL3223608;DTXSID20454187;AWVUYKHSNNYPOX-MXWKQRLJSA-N;AKOS005264656;Cyclohexanecarbonitrile, 5-methyl-2-(1-methylethyl)-, (1S,2S,5R)- (9CI);(1R,3S,4S)-p-Menthane-3-carbonitrile;(1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonitrile

Suppliers and Price of (1S,2S,5R)-Neomenthyl cyanide

Supply Marketing:Edit

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

TRC
(1S,2S,5R)-Neomenthylcyanide
100mg
$ 75.00

Matrix Scientific
(1S,2S,5R)-Neomenthyl cyanide
1g
$ 100.00

American Custom Chemicals Corporation
(1S,2S,5R)-NEOMENTHYL CYANIDE 95.00%
1G
$ 255.15

AK Scientific
(1S,2S,5R)-Neomenthylcyanide
1g
$ 185.00

Total 10 raw suppliers

Chemical Property of (1S,2S,5R)-Neomenthyl cyanide Edit

Chemical Property:

PSA：23.79000
LogP:3.21838
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:165.151749610
Heavy Atom Count:12
Complexity:186

Purity/Quality:

98% ^*data from raw suppliers

(1S,2S,5R)-Neomenthylcyanide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC(C(C1)C#N)C(C)C
Isomeric SMILES:C[C@@H]1CC[C@H]([C@H](C1)C#N)C(C)C

Technology Process of (1S,2S,5R)-Neomenthyl cyanide

There total 5 articles about (1S,2S,5R)-Neomenthyl cyanide 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: 99.0%