2,3-Thiophenedimethanol

Base Information

Chemical Name:2,3-Thiophenedimethanol
CAS No.:13250-85-6
Molecular Formula:C₆H₈O₂S
Molecular Weight:144.194
Hs Code.:
European Community (EC) Number:966-039-9
DSSTox Substance ID:DTXSID301313996

Synonyms:13250-85-6;2,3-Thiophenedimethanol;Thiophene-2,3-diyldimethanol;thiene-2,3-diyldimethanol;[2-(HYDROXYMETHYL)THIOPHEN-3-YL]METHANOL;MFCD06202801;Thiophene-2,3-dimethanol;bis-hydroxymethylthiophene;[3-(HYDROXYMETHYL)THIOPHEN-2-YL]METHANOL;SCHEMBL2690986;DTXSID301313996;AKOS005144511;[2-(hydroxymethyl)-3-thienyl]methanol;AS-58016;SY246810;CS-0444689;EN300-201457;W18906;A928968

Suppliers and Price of 2,3-Thiophenedimethanol

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
Thiene-2,3-Diyldimethanol
100mg
$ 175.00

TRC
Thiene-2,3-Diyldimethanol
50mg
$ 110.00

Crysdot
Thiophene-2,3-diyldimethanol 97%
1g
$ 790.00

Arctom
Thiophene-2,3-diyldimethanol 97%
1g
$ 606.00

AK Scientific
2,3-Thiophenedimethanol
5g
$ 1072.00

Total 4 raw suppliers

Chemical Property of 2,3-Thiophenedimethanol

Chemical Property:

XLogP3:-0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:144.02450067
Heavy Atom Count:9
Complexity:87.1

Purity/Quality:

97% ^*data from raw suppliers

Thiene-2,3-Diyldimethanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CSC(=C1CO)CO

Technology Process of 2,3-Thiophenedimethanol

There total 5 articles about 2,3-Thiophenedimethanol 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: 88.0%

: 1451-95-2
thiophene-2,3-dicarboxylic acid

: 13250-85-6
2,3-bis(hydroxymethyl)thiophene

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 24h; Heating;
DOI:10.1016/S0040-4039(00)96870-9

Reference yield: 74.0%

: 13250-85-6
2,3-bis(hydroxymethyl)thiophene

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 17h; Inert atmosphere; Reflux;

Reference yield:

: 527-72-0
2-thiophenylcarboxylic acid

: 13250-85-6
2,3-bis(hydroxymethyl)thiophene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) nBuLi; 2.) aq.HCl / 1.) THF, -78 deg C, O_.5 h

2: 88 percent / LiAlH₄ / tetrahydrofuran / 24 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; In tetrahydrofuran;
DOI:10.1016/S0040-4039(00)96870-9