Structure

3-Formylthiophene-2-boronic acid

CAS
17303-83-2
Catalog Number
ACM17303832
Category
Boronic Acids
Molecular Weight
155.97
Molecular Formula
C5H5BO3S

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Specification

Synonyms
3-Formyl-2-thiopheneboronic acid; 3-Formylthiophene-2-boronic acid; (3-Formylthiophen-2-yl)boronic acid; (3-formylthiophen-2-yl)boronic acid;
IUPAC Name
(3-formylthiophen-2-yl)boronic acid
SMILES
B(C1=C(C=CS1)C=O)(O)O
InChI Key
HYXMHAHVUFTVFZ-UHFFFAOYSA-N
Boiling Point
381.2ºC at 760mmHg
Melting Point
330ºC
Flash Point
184.4ºC
Density
1.41g/cm³
Exact Mass
156.00500
H-Bond Acceptor
4
H-Bond Donor
2
Safety Description
S26-S36
WGK Germany
3
What is the molecular formula of 3-Formylthiophene-2-boronic acid?

The molecular formula of 3-Formylthiophene-2-boronic acid is C5H5BO3S.

What is the molecular weight of 3-Formylthiophene-2-boronic acid?

The molecular weight of 3-Formylthiophene-2-boronic acid is 155.97 g/mol.

What is the IUPAC name of 3-Formylthiophene-2-boronic acid?

The IUPAC name of 3-Formylthiophene-2-boronic acid is (3-formylthiophen-2-yl)boronic acid.

What is the InChI of 3-Formylthiophene-2-boronic acid?

The InChI of 3-Formylthiophene-2-boronic acid is InChI=1S/C5H5BO3S/c7-3-4-1-2-10-5(4)6(8)9/h1-3,8-9H.

What is the InChIKey of 3-Formylthiophene-2-boronic acid?

The InChIKey of 3-Formylthiophene-2-boronic acid is HYXMHAHVUFTVFZ-UHFFFAOYSA-N.

What is the canonical SMILES of 3-Formylthiophene-2-boronic acid?

The canonical SMILES of 3-Formylthiophene-2-boronic acid is B(C1=C(C=CS1)C=O)(O)O.

What is the CAS number of 3-Formylthiophene-2-boronic acid?

The CAS number of 3-Formylthiophene-2-boronic acid is 17303-83-2.

What is the European Community (EC) number of 3-Formylthiophene-2-boronic acid?

The European Community (EC) number of 3-Formylthiophene-2-boronic acid is 681-376-9.

What is the ChEMBL ID of 3-Formylthiophene-2-boronic acid?

The ChEMBL ID of 3-Formylthiophene-2-boronic acid is CHEMBL334932.

Is 3-Formylthiophene-2-boronic acid a canonicalized compound?

Yes, 3-Formylthiophene-2-boronic acid is a canonicalized compound.

Downstream Synthesis Route 1

  • 17303-83-2
  • 71637-34-8
  • 222840-73-5

Reference: [1] Journal of Medicinal Chemistry, 2010, vol. 53, # 5, p. 2227 - 2238

Downstream Synthesis Route 2

  • 17303-83-2
  • 222840-73-5

Reference: [1] Patent: US6034089, 2000, A,

Downstream Synthesis Route 3

  • 33906-30-8
  • 17303-83-2
  • 17303-90-1

Reference: [1]Acta Chemica Scandinavica (1947),1967,vol. 21,p. 2151 - 2166

Downstream Synthesis Route 4

  • 17303-83-2
  • 17303-84-3

Reference: [1]Gronowitz,S.; Namtvedt,J.
[Acta Chemica Scandinavica (1947), 1967, vol. 21, p. 2151 - 2166]

Downstream Synthesis Route 5

  • 17303-83-2
  • 100-63-0
  • 17303-86-5

Reference: [1]Gronowitz,S.; Namtvedt,J.
[Acta Chemica Scandinavica (1947), 1967, vol. 21, p. 2151 - 2166]
[Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: B: B-Verb.1, 2.9.6, page 202 - 206]
[2]Gronowitz,S.; Namtvedt,J.
[Acta Chemica Scandinavica (1947), 1967, vol. 21, p. 2151 - 2166]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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