Structure

2-Bromobenzaldehyde

CAS
6630-33-7
Catalog Number
ACM6630337
Category
Bromine Series

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What is the molecular formula of 2-Bromobenzaldehyde?

The molecular formula of 2-Bromobenzaldehyde is C7H5BrO.

What is the molecular weight of 2-Bromobenzaldehyde?

The molecular weight of 2-Bromobenzaldehyde is 185.02 g/mol.

What is the IUPAC name of 2-Bromobenzaldehyde?

The IUPAC name of 2-Bromobenzaldehyde is 2-bromobenzaldehyde.

What is the InChI of 2-Bromobenzaldehyde?

The InChI of 2-Bromobenzaldehyde is InChI=1S/C7H5BrO/c8-7-4-2-1-3-6(7)5-9/h1-5H.

What is the InChIKey of 2-Bromobenzaldehyde?

The InChIKey of 2-Bromobenzaldehyde is NDOPHXWIAZIXPR-UHFFFAOYSA-N.

What is the canonical SMILES of 2-Bromobenzaldehyde?

The canonical SMILES of 2-Bromobenzaldehyde is C1=CC=C(C(=C1)C=O)Br.

What is the CAS number of 2-Bromobenzaldehyde?

The CAS number of 2-Bromobenzaldehyde is 6630-33-7.

What is the EC number of 2-Bromobenzaldehyde?

The EC number of 2-Bromobenzaldehyde is 229-622-2.

What is the ChEMBL ID of 2-Bromobenzaldehyde?

The ChEMBL ID of 2-Bromobenzaldehyde is CHEMBL3236916.

Is 2-Bromobenzaldehyde a canonicalized compound?

Yes, 2-Bromobenzaldehyde is a canonicalized compound.

Downstream Synthesis Route 1

  • 50-01-1
  • 6630-33-7
  • 1687-51-0

Reference: [1] Synthesis, 2009, # 16, p. 2679 - 2688

Downstream Synthesis Route 2

  • 1692-25-7
  • 6630-33-7
  • 176690-44-1

Reference: [1] Patent: EP2123637, 2009, A1, . Location in patent: Page/Page column 106

Downstream Synthesis Route 3

  • 6630-33-7
  • 1532-72-5

Reference: [1] Heterocycles, 1986, vol. 24, # 8, p. 2311 - 2314

Downstream Synthesis Route 4

  • 16357-40-7
  • 6630-33-7
  • 72739-47-0

Reference: [1]Journal of Medicinal Chemistry,1980,vol. 23,p. 335 - 338

Downstream Synthesis Route 5

  • 151-50-8
  • 517-21-5
  • 6630-33-7
  • 98769-16-5

Reference: [1]Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry,1985,vol. 24,p. 268 - 272

Downstream Synthesis Route 6

  • 6630-33-7
  • 2682-45-3
  • 102912-68-5

Reference: [1]Journal fur praktische Chemie (Leipzig 1954),1985,vol. 327,p. 698 - 704

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

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