(R)-(-)-2-Heptanol

Base Information Edit

Chemical Name:(R)-(-)-2-Heptanol
CAS No.:6033-24-5
Molecular Formula:C7H16O
Molecular Weight:116.203
Hs Code.:2905199090
European Community (EC) Number:624-710-0
UNII:Z96RWD50O7
Nikkaji Number:J52.599E
Wikidata:Q27295180
Metabolomics Workbench ID:3335
Mol file:6033-24-5.mol

Synonyms:(R)-(-)-2-Heptanol;(R)-Heptan-2-ol;6033-24-5;(2R)-heptan-2-ol;2-Heptanol, (R)-;Heptan-2R-ol;(R)-2-heptanol;2-Heptanol, (-)-;(-)-2-heptanol;UNII-Z96RWD50O7;Z96RWD50O7;2-Heptanol, (2R)-;L-2-HYDROXYHEPTANE;L-AMYLMETHYLCARBINOL;SCHEMBL1261897;BDBM36164;CHEBI:179176;AMY25723;(R)-(-)-2-Heptanol, 95%;LMFA05000477;MFCD00065956;2-HEPTANOL (2R)-FORM [MI];AKOS016015016;AS-76029;CS-0152365;D83253;EN300-1831936;Q27295180

Suppliers and Price of (R)-(-)-2-Heptanol

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
(R)-(-)-2-Heptanol
100mg
$ 50.00

Crysdot
(R)-Heptan-2-ol 95+%
5g
$ 520.00

American Custom Chemicals Corporation
(R)-(-)-2-HEPTANOL 95.00%
1G
$ 289.80

Ambeed
(R)-Heptan-2-ol 95%
1g
$ 148.00

Ambeed
(R)-Heptan-2-ol 95%
250mg
$ 63.00

Ambeed
(R)-Heptan-2-ol 95%
100mg
$ 42.00

Ambeed
(R)-Heptan-2-ol 95%
5g
$ 439.00

AHH
(R)-(-)-2-Heptanol 95%
5g
$ 298.00

Total 37 raw suppliers

Chemical Property of (R)-(-)-2-Heptanol Edit

Chemical Property:

Appearance/Colour:Colorless to light yellow liquid
Melting Point:-30.45°C (estimate)
Refractive Index:n20/D 1.419(lit.)
Boiling Point:159.4 °C at 760 mmHg
PKA:15.44±0.20(Predicted)
Flash Point:64 ºC
PSA：20.23000
Density:0.818 g/cm³
LogP:1.94750
Storage Temp.:2-8°C
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:116.120115130
Heavy Atom Count:8
Complexity:43.7

Purity/Quality:

99% ^*data from raw suppliers

(R)-(-)-2-Heptanol ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn, Xi
Hazard Codes:Xn,Xi
Statements: 21-37/38-41
Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCCCCC(C)O
Isomeric SMILES:CCCCC[C@@H](C)O
Uses (R)-(-)-2-Heptanol is used in preparation of triazole carbamate pyridyl sulfonamides as LPA receptor antagonists and uses thereof.

Technology Process of (R)-(-)-2-Heptanol

There total 15 articles about (R)-(-)-2-Heptanol 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:

: 142-82-5
n-heptane

: 62701-49-9
(3R)-heptan-3-ol

: 26549-25-7
S-(+)-3-heptanol

: 6033-23-4
(S)-2-heptanol

: 6033-24-5
(R)-2-heptanol

: 589-55-9
heptan-4-ol

Guidance literature:: With NADH dependent P₄₅₀BM₃ monooxygenase 19A 12 from Bacillus megaterium; oxygen; NADH; catalase; In aq. phosphate buffer; ethanol; at 20 ℃; pH=8; enantioselective reaction; Catalytic behavior; Enzymatic reaction;
DOI:10.1002/adsc.201300143

Reference yield:

: 14925-96-3,56052-93-8,56740-07-9,115667-91-9,115667-92-0,149117-08-8,149117-12-4
cis-2,3-epoxyheptane

: 589-82-2
heptan-3-ol

: 6033-24-5
(R)-2-heptanol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether;
DOI:10.1016/0040-4039(96)01935-1

Reference yield:

: 142-82-5
n-heptane

: 110-43-0
n-pentyl methyl ketone

: 589-82-2
heptan-3-ol

: 6033-23-4
(S)-2-heptanol

: 6033-24-5
(R)-2-heptanol

Guidance literature:: With D-glucose; E_. coli flavodoxin reductase; flavodoxin YkuN from Bacillus subtilis; glucose dehydrogenase from B_. megaterium; P₄₅₀ monooxygenase from Nocardia farcinica; NADPH; bovine serum albumin; catalase from bovine liver; In ethanol; at 25 ℃; for 24h; Solvent; stereoselective reaction; Catalytic behavior; Kinetics; Enzymatic reaction;
DOI:10.1039/c4cc00647j