(S)-1,5-Dimethylhexylamine

Base Information

Chemical Name:(S)-1,5-Dimethylhexylamine
CAS No.:70419-10-2
Molecular Formula:C₈H₁₉N
Molecular Weight:129.246
Hs Code.:2921199090
European Community (EC) Number:274-598-9
UNII:WC7H88R84F
Nikkaji Number:J61.832B
Mol file:70419-10-2.mol

Synonyms:70419-10-2;(2S)-6-methylheptan-2-amine;(S)-1,5-Dimethylhexylamine;Octodrine, (S)-;2-Heptanamine,6-methyl-, (2S)-;(S)-2-AMINO-6-METHYLHEPTANE;WC7H88R84F;EINECS 274-598-9;UNII-WC7H88R84F;SCHEMBL2253652;(S)-2-amino-6-methyl heptane;[S,(+)]-1,5-Dimethylhexylamine;AKOS006359945;(2S)-6-METHYL-2-HEPTANAMINE;(S)-(+)-6-METHYL-2-HEPTYLAMINE;2-HEPTANAMINE, 6-METHYL-, (2S)-;EN300-1836613

Suppliers and Price of (S)-1,5-Dimethylhexylamine

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

TRC
(S)-2-Amino-6-methylheptane
100mg
$ 220.00

TRC
(S)-2-Amino-6-methylheptane
50mg
$ 155.00

American Custom Chemicals Corporation
(S)-2-AMINO-6-METHYLHEPTANE 95.00%
10G
$ 1382.48

American Custom Chemicals Corporation
(S)-2-AMINO-6-METHYLHEPTANE 95.00%
5G
$ 955.42

American Custom Chemicals Corporation
(S)-2-AMINO-6-METHYLHEPTANE 95.00%
1G
$ 646.25

Total 8 raw suppliers

Chemical Property of (S)-1,5-Dimethylhexylamine

Chemical Property:

Melting Point:11.43°C (estimate)
Refractive Index:1.4148 (estimate)
Boiling Point:155 °C at 760 mmHg
Flash Point:48.9 °C
PSA：26.02000
Density:0.783 g/cm³
LogP:2.47010
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:129.151749610
Heavy Atom Count:9
Complexity:59.6

Purity/Quality:

99% ^*data from raw suppliers

(S)-2-Amino-6-methylheptane ^*data from reagent suppliers

Safty Information:

Pictogram(s): R10:Flammable.; R36/37/38:Irritating to eyes, respiratory system and skin.;
Hazard Codes: Xi:Irritant;
Statements: R10:Flammable.; R36/37/38:Irritating to eyes, respiratory system and skin.;
Safety Statements: S16:Keep away from sources of ignition - No smoking.; S26:In case of contact with eyes, rinse immediately with plenty of

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCCC(C)N
Isomeric SMILES:C[C@@H](CCCC(C)C)N

Technology Process of (S)-1,5-Dimethylhexylamine

There total 21 articles about (S)-1,5-Dimethylhexylamine 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: 52.0%

: 543-82-8,70419-10-2
1,5-dimethylhexylamine

: 1100753-75-0
N-octanoylglycine 2,2,2-trifluoroethyl ester

: 70419-11-3,70419-10-2
(R)-6-methylheptan-2-amine

: 1100754-06-0
N-(((S)-6-methylheptan-2-ylcarbamoyl)methyl)octanamide

Guidance literature:: With Alkaline protease; In 3-methylpentan-3-ol; at 20 ℃; for 4h; optical yield given as %ee; Enzymatic reaction;
DOI:10.1039/b812089g

Reference yield: 47.0%

: 543-82-8,70419-10-2
1,5-dimethylhexylamine

: 1222802-05-2
N-octanoyl-L-alanine 2,2,2-trifluoroethyl ester

: 70419-10-2
C₈H₁₉N

: 1244047-15-1
N-((S)-1-((S)-6-methylheptan-2-ylcarbamoyl)ethyl)octanamide

Guidance literature:: With Bacillus licheniformis alkaline protease; In tert-butyl alcohol; at 30 ℃; for 1.5h; optical yield given as %ee; Enzymatic reaction;
DOI:10.1039/c0ob00054j

Reference yield: 33.0%

: 543-82-8,70419-10-2
1,5-dimethylhexylamine

: 1384127-07-4
N-octanoyl dimethyl glycine trifluoroethyl ester

: 70419-10-2
(S)-6-methylheptan-2-amine

: 70419-11-3,70419-10-2
(R)-6-methylheptan-2-amine

: 1384127-18-7
N-(2-methyl-1-(6-methylheptan-2-ylamino)-1-oxopropan-2-yl)octanamide

Guidance literature:: With coated protease; In 3-methylpentan-3-ol; at 21 ℃; for 144h; enantioselective reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/adsc.201100993