(S)-2-Bromooctane

Base Information Edit

Chemical Name:(S)-2-Bromooctane
CAS No.:1191-24-8
Molecular Formula:C8H17Br
Molecular Weight:193.127
Hs Code.:2903399090
UNII:A3A2KWD38T
DSSTox Substance ID:DTXSID40152315
Nikkaji Number:J10.695J
Wikidata:Q27273556
Mol file:1191-24-8.mol

Synonyms:(S)-2-BROMOOCTANE;1191-24-8;(+)-2-Bromooctane;sec-Octyl bromide, (+)-;(2S)-2-BROMOOCTANE;(S)-2-Octyl bromide;Octane, 2-bromo-, (S)-;(+)-2-Octyl bromide;Octane, 2-bromo-, l-;(S)-(+)-2-Bromooctane;Octane, 2-bromo-, (2S)-;UNII-A3A2KWD38T;A3A2KWD38T;[S,(+)]-2-Bromooctane;(s)-2-bromo-octane;sec-Octyl bromide (S)-form [MI];Octane, 2-bromo-, (S)-(+)-;(+)-sec-octyl bromide;SCHEMBL3673764;DTXSID40152315;AKOS006344569;AKOS015833983;Q27273556

Suppliers and Price of (S)-2-Bromooctane

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

American Custom Chemicals Corporation
(S)-2-BROMOOCTANE 95.00%
1G
$ 867.12

Total 12 raw suppliers

Chemical Property of (S)-2-Bromooctane Edit

Chemical Property:

PSA：0.00000
LogP:3.74020
XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:5
Exact Mass:192.05136
Heavy Atom Count:9
Complexity:52.5

Purity/Quality:

98%,99%, ^*data from raw suppliers

(S)-2-BROMOOCTANE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(C)Br
Isomeric SMILES:CCCCCC[C@H](C)Br

Technology Process of (S)-2-Bromooctane

There total 14 articles about (S)-2-Bromooctane 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: 97.0%

: 5978-70-1,113301-48-7,4128-32-9
(R)-Octan-2-ol

: 1191-24-8
(S)-(+)-2-bromooctane

Guidance literature:: With 1,2-bis (triphenylphosphino)ethane tetrabromide; In dichloromethane; at 23 ℃; for 0.25h;
DOI:10.1016/S0040-4039(01)80984-9

Reference yield: 95.0%

: 5978-70-1,113301-48-7,4128-32-9
l-2-octanol

: 1191-24-8
d-2-bromooctane

Guidance literature:: With 1,1,1,2,2,2-hexamethyldisilane; pyridinium hydrobromide perbromide; In chloroform; at 25 ℃; for 96h;
DOI:10.1021/jo01297a020

Reference yield: 90.0%

: 73472-49-8
(R)-N,N-dimethyl-2-<<(1-methylheptyl)oxy>sulfonyl>ethanaminium bromide

: 1191-24-8
(S)-(+)-2-bromooctane

Guidance literature:: In benzene; at 80 ℃; for 1h; Product distribution; stereochemistry of reactions of 1-methylheptyl betylates, percentage inversion; preparative nucleophilic substitution by way of <2>-, <3>-, and <4>betylates; substrate-reagent ion-pair (SRIP) reactions of betylates;
DOI:10.1021/ja00389a038