1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one, 97%

Name: 1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one, 97% | 4424-80-0
Brand: J&K Chemical
SKU: JK227191_1_G
Price: 8.5 USD
Availability: OutOfStock

Cat. No JK227191_1_G

Vendor: J&K Chemical

Product Information

Product Name

1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one, 97%

Brand Name

J&K

Product Number

227191

CAS

4424-80-0

Molecular Formula

C10H11NO

Molecular Weight

161.20

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

4,5-Dihydro-1H-benzobazepin-2(3H)-one
1,3,4,5-Tetrahydrobenzobazepin-2-one

PubChem CID

248580

IUPAC Name

1,3,4,5-tetrahydro-1-benzazepin-2-one

InChI Key

HRVRAYIYXRVAPR-UHFFFAOYSA-N

SMILES

C1CC2=CC=CC=C2NC(=O)C1

Properties

Melting Point

141-145

Boiling Point

339

Safety Information

GHS Symbols

Signal Word

Warning

Hazard Statement

H302

H317

Precautionary Statement

P301+P312+P330

P302+P352

P333+P313

P362+P364

P501

Storage Condition

Store at 2-8℃

References

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

Publication Name: Biochemical and Biophysical Research Communications

Publication Date: 2023-10-30

DOI: 10.1016/j.bbrc.2023.08.050

Ring expansion of donor—acceptor cyclopropanes bearing arylcarbamoyl group into 1,5-diarylpyrrolidin-2-ones

Publication Name: Russian Chemical Bulletin

Publication Date: 2022-11

DOI: 10.1007/s11172-022-3671-3

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

Publication Name: The Journal of biological chemistry

Publication Date: 2022-08

DOI: 10.1016/j.jbc.2022.102228

The Reaction of Ketoximes with Hypervalent Iodine Reagents: Beckmann Rearrangement and Hydrolysis to Ketones

Publication Name: Synthesis

Publication Date: 2022-06-08

DOI: 10.1055/a-1835-2188

A convenient approach to the synthesis of 1-halomethyl-substituted 2,4,5,6-tetrahydro-1H-imidazo[1,2-a][1]benzazepines

Publication Name: Chemistry of Heterocyclic Compounds

Publication Date: 2021-12

DOI: 10.1007/s10593-021-03042-x

1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one, 97%

Product Information

General Information

Properties

Safety Information

References

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

Ring expansion of donor—acceptor cyclopropanes bearing arylcarbamoyl group into 1,5-diarylpyrrolidin-2-ones

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

The Reaction of Ketoximes with Hypervalent Iodine Reagents: Beckmann Rearrangement and Hydrolysis to Ketones

A convenient approach to the synthesis of 1-halomethyl-substituted 2,4,5,6-tetrahydro-1H-imidazo[1,2-a][1]benzazepines