2-Amino-4-bromobenzothiazole

• CAS: 20358-02-5
• Catalog Number: ACM20358025
• Category: Bromine Series
• Molecular Weight: 229.097
• Molecular Formula: C₇H₅BrN₂S

Custom Q&A

What is the molecular formula of 2-Amino-4-bromobenzothiazole?

The molecular formula of 2-Amino-4-bromobenzothiazole is C7H5BrN2S.

What is the synonym for 2-Amino-4-bromobenzothiazole?

One of the synonyms for 2-Amino-4-bromobenzothiazole is 4-Bromobenzo[d]thiazol-2-amine.

When was 2-Amino-4-bromobenzothiazole created?

2-Amino-4-bromobenzothiazole was created on July 14, 2005.

What is the IUPAC name of 2-Amino-4-bromobenzothiazole?

The IUPAC name of 2-Amino-4-bromobenzothiazole is 4-bromo-1,3-benzothiazol-2-amine.

What is the InChI of 2-Amino-4-bromobenzothiazole?

The InChI of 2-Amino-4-bromobenzothiazole is InChI=1S/C7H5BrN2S/c8-4-2-1-3-5-6(4)10-7(9)11-5/h1-3H,(H2,9,10).

What is the InChIKey of 2-Amino-4-bromobenzothiazole?

The InChIKey of 2-Amino-4-bromobenzothiazole is FVMCARDEQKVVIS-UHFFFAOYSA-N.

What is the canonical SMILES of 2-Amino-4-bromobenzothiazole?

The canonical SMILES of 2-Amino-4-bromobenzothiazole is C1=CC2=C(C(=C1)Br)N=C(S2)N.

What is the CAS number of 2-Amino-4-bromobenzothiazole?

The CAS number of 2-Amino-4-bromobenzothiazole is 20358-02-5.

What is the molecular weight of 2-Amino-4-bromobenzothiazole?

The molecular weight of 2-Amino-4-bromobenzothiazole is 229.10 g/mol.

How many hydrogen bond acceptor atoms are there in 2-Amino-4-bromobenzothiazole?

There are 3 hydrogen bond acceptor atoms in 2-Amino-4-bromobenzothiazole.

Synthetic Use

Upstream Synthesis Route 1

• 5391-30-0

• 20358-02-5

Reference: [1] Medicinal Chemistry Research, 2012, vol. 21, # 7, p. 1136 - 1148
[2] Patent: WO2010/142402, 2010, A1, . Location in patent: Page/Page column 114-115
[3] Journal fuer Praktische Chemie (Leipzig), 1974, vol. 316, p. 154 - 158
[4] Journal of the Chemical Society [Section] C: Organic, 1969, p. 268 - 272

Upstream Synthesis Route 2

• 615-36-1

• 20358-02-5

Reference: [1] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 8, p. 1759 - 1775

Upstream Synthesis Route 3

• 333-20-0
• 615-36-1

• 20358-02-5

Reference: [1] Synlett, 2012, vol. 23, # 15, p. 2219 - 2222
[2] European Journal of Medicinal Chemistry, 2013, vol. 67, p. 1 - 13

Upstream Synthesis Route 4

• 5391-30-0

• 20358-02-5

Reference: [1]Medicinal Chemistry Research,2012,vol. 21,p. 1136 - 1148
[2]Patent: WO2010/142402,2010,A1 .Location in patent: Page/Page column 114-115
[3]Journal fur praktische Chemie (Leipzig 1954),1974,vol. 316,p. 154 - 158
[4]Journal of the Chemical Society C: Organic,1969,p. 268 - 272

Upstream Synthesis Route 5

• 615-36-1

• 20358-02-5

Reference: [1]Journal of the Chemical Society C: Organic,1969,p. 268 - 272