(4S)-2-Methyl-2,4-pentanediol

Base Information

Chemical Name:(4S)-2-Methyl-2,4-pentanediol
CAS No.:99210-91-0
Molecular Formula:C₆H₁₄O₂
Molecular Weight:118.176
Hs Code.:2905399590
European Community (EC) Number:602-057-2
DSSTox Substance ID:DTXSID601308225
Nikkaji Number:J766.306D
Wikidata:Q27094497
Metabolomics Workbench ID:56543
Mol file:99210-91-0.mol

Synonyms:C.I. acid fast red 360;telon fast red AFG

Suppliers and Price of (4S)-2-Methyl-2,4-pentanediol

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

Total 9 raw suppliers

Chemical Property of (4S)-2-Methyl-2,4-pentanediol

Chemical Property:

Boiling Point:87-90 °C(Press: 6 Torr)
PKA:15.10±0.29(Predicted)
Density:0.960±0.06 g/cm3(Predicted)
XLogP3:0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:118.099379685
Heavy Atom Count:8
Complexity:68.9

Purity/Quality:: 99%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of (4S)-2-Methyl-2,4-pentanediol

There total 2 articles about (4S)-2-Methyl-2,4-pentanediol 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:

: 107-41-5
2-methyl-2,4-pentanediol

: 99210-91-0
(S)-2-methyl-2,4-pentanediol

: 99210-90-9
Hexylene glycol

Guidance literature:: With Ni2(L-asp)2(4,4′-bipyridine); at 200 ℃; for 240h; under 750.075 Torr; Temperature; Pressure; enantioselective reaction; Resolution of racemate; Sonication;
DOI:10.1039/c3cc42376j