Tolvaptan Impurity 19

Name: Tolvaptan Impurity 19 | 933-88-0
Brand: US-CATO
SKU: S57C4X-195519_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57C4X-195519_10_MG

Vendor: US-CATO

Product Information

Product Name

Tolvaptan Impurity 19

Brand Name

US-CATO

Product Number

C4X-195519

CAS

933-88-0

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

70276

IUPAC Name

2-methylbenzoyl chloride

InChI Key

GPZXFICWCMCQPF-UHFFFAOYSA-N

SMILES

CC1=CC=CC=C1C(=O)Cl

References Data Source From Pubchem

2-Fluorocordycepin: Chemoenzymatic Synthesis and Study of Anticancer Activities In Vitro

Publication Name: Russian Journal of Bioorganic Chemistry

Publication Date: 2025-06

DOI: 10.1134/s1068162025601144

A fluorescent turn-on probe based on coumarin-thiourea conjugate for Hg2+ detection in a wide pH range

Publication Name: Chemical Papers

Publication Date: 2023-03-20

DOI: 10.1007/s11696-023-02778-4

Synthesis of Heteroatoms Including at Least One Boron Metal Complexes and Their Catalytic Applications

Publication Name: Multifunctional Boron-Nitride Composites

Publication Date: 2023

DOI: 10.1007/978-981-99-2866-8_2

Synthesis, Biological and Acidic Properties of Some New 2-Ethoxy-4-[(3-alkyl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethine]-phenyl 2-Methylbenzoate Derivatives

Publication Name: Moscow University Chemistry Bulletin

Publication Date: 2022-12

DOI: 10.3103/s0027131422070070

Acylation and Arylation of 6-Amino-4-methylquinolin-2(1H)-one

Publication Name: Science of Synthesis

Publication Date: 2022

Tolvaptan Impurity 19

Product Information

General Information

References Data Source From Pubchem

2-Fluorocordycepin: Chemoenzymatic Synthesis and Study of Anticancer Activities In Vitro

A fluorescent turn-on probe based on coumarin-thiourea conjugate for Hg2+ detection in a wide pH range

Synthesis of Heteroatoms Including at Least One Boron Metal Complexes and Their Catalytic Applications

Synthesis, Biological and Acidic Properties of Some New 2-Ethoxy-4-[(3-alkyl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethine]-phenyl 2-Methylbenzoate Derivatives

Acylation and Arylation of 6-Amino-4-methylquinolin-2(1H)-one