2-Octanol, acetate, (R)-

Base Information

Chemical Name:2-Octanol, acetate, (R)-
CAS No.:54712-18-4
Molecular Formula:C10H20O2
Molecular Weight:172.268
Hs Code.:
UNII:EY56S72U9R
Nikkaji Number:J67.260B

Synonyms:(r)-2-octyl acetate;2-Octanol, acetate, (R)-;(-)-2-Acetoxyoctane;(-)-2-Octyl acetate;2-Octyl acetate, (-)-;2-Octyl acetate, (2R)-;EY56S72U9R;(R)-(-)-1-Methylheptyl acetate;UNII-EY56S72U9R;54712-18-4;SCHEMBL4602055;acetic acid (r)-(-)-1-methyl-heptyl ester

Suppliers and Price of 2-Octanol, acetate, (R)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Octanol, acetate, (R)-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:172.146329876
Heavy Atom Count:12
Complexity:121

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(C)OC(=O)C
Isomeric SMILES:CCCCCC[C@@H](C)OC(=O)C

Technology Process of 2-Octanol, acetate, (R)-

There total 12 articles about 2-Octanol, acetate, (R)- 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: 49.0%

: 85-44-9
phthalic anhydride

: 108-05-4,9003-20-7
vinyl acetate

: 4128-31-8,113301-48-7,4128-32-9
rac-octan-2-ol

: 54712-18-4
(R)-2-octyl acetate

: 6114-64-3
2-{[(S)-octan-7-yloxy]carbonyl}benzoic acid

Guidance literature:: vinyl acetate; rac-octan-2-ol; In dichloromethane; at 20 ℃; for 16h; Inert atmosphere; Enzymatic reaction;

phthalic anhydride; With triethylamine; In dichloromethane; for 7h; optical yield given as %ee; enantioselective reaction; Reflux; Inert atmosphere;
DOI:10.1055/s-0029-1216997

Reference yield: 48.7%

: 108-05-4,9003-20-7
vinyl acetate

: 4128-31-8,113301-48-7,4128-32-9
rac-octan-2-ol

: 6169-06-8,113301-48-7,4128-32-9
(S)-2-Octanol

: 54712-18-4
(R)-2-octyl acetate

Guidance literature:: With sol-gel encapsulated Candida antarctica lipase SP 525; at 20 ℃; for 17h;
DOI:10.1271/bbb.66.221

Reference yield:

: 26735-84-2
oct-1-en-2-yl acetate

: 4128-31-8,113301-48-7,4128-32-9
rac-octan-2-ol

: 54712-18-4
(R)-2-octyl acetate

: 3540-05-4
(S)-1-methylheptyl acetate

: 111-13-7
hexyl-methyl-ketone

Guidance literature:: With Novozym 435; 2,6-dimethyl-4-heptanol; (Ph4C4CO)2H(μ-H)(CO)4Ru2; In toluene; at 70 ℃; for 68h; Title compound not separated from byproducts.; Enzymatic reaction;
DOI:10.1021/ol9914043