2-Formyl-4-(thiophen-3-YL)phenol

Base Information

Chemical Name:2-Formyl-4-(thiophen-3-YL)phenol
CAS No.:298220-86-7
Molecular Formula:C₁₁H₈O₂S
Molecular Weight:204.249
Hs Code.:
ChEMBL ID:CHEMBL3660409
DSSTox Substance ID:DTXSID00602407
Wikidata:Q82499458

Synonyms:298220-86-7;2-FORMYL-4-(THIOPHEN-3-YL)PHENOL;2-Hydroxy-5-(3-thienyl)benzaldehyde;2-Hydroxy-5-(thien-3-yl)benzaldehyde;2-Hydroxy-5-(thiophen-3-yl)benzaldehyde;SCHEMBL6639987;CHEMBL3660409;DTXSID00602407;RUICYUGGZYRQOG-UHFFFAOYSA-N;BDBM111257;MFCD06802126;2-hydroxy-5-thiophen-3-ylbenzaldehyde;AKOS004116227;2-Formyl-4-(thiophen-3-yl)phenol, 95%;DB-347120;US8614253, 43-17

Suppliers and Price of 2-Formyl-4-(thiophen-3-YL)phenol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-Formyl-4-(thiophen-3-YL)phenol

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:204.02450067
Heavy Atom Count:14
Complexity:208

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1C2=CSC=C2)C=O)O

Technology Process of 2-Formyl-4-(thiophen-3-YL)phenol

There total 1 articles about 2-Formyl-4-(thiophen-3-YL)phenol 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: 98.0%

: 6165-69-1
Thien-3-ylboronic acid

: 1761-61-1
5-bromosalicyclaldehyde

: 298220-86-7
2-hydroxy-5-(thiophen-3-yl)benzaldehyde

Guidance literature:: With [Pd(N-(3-chloro-2-quinoxalinyl)-N'-(2,6-diisopropylphenyl)imidazolium)(PPh₃)Cl₂]; potassium carbonate; In water; at 70 ℃; for 3h; Catalytic behavior;
DOI:10.1039/c7dt01433c

Reference yield: 71.0%

: 298220-86-7
2-hydroxy-5-(thiophen-3-yl)benzaldehyde

: 1451929-24-0
C₂₃H₂₆N₂

: C₃₄H₃₄N₂OS

Guidance literature:: With sodium cyanoborohydride; In tetrahydrofuran; methanol; acetic acid; at 20 ℃; for 24h; Schlenk technique; Inert atmosphere; Molecular sieve;
DOI:10.1002/adsc.201500495