1313028-09-9

Basic information

• Product Name: ortho-(cyclopropylethynyl)benzoic acid
• Synonyms: ortho-(cyclopropylethynyl)benzoic acid
• CAS NO: 1313028-09-9
• Molecular Weight: 186.21
• Mol File: 1313028-09-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: ortho-(cyclopropylethynyl)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: ortho-(cyclopropylethynyl)benzoic acid(1313028-09-9)
• EPA Substance Registry System: ortho-(cyclopropylethynyl)benzoic acid(1313028-09-9)

Safety Data

• Hazardous Substances Data: 1313028-09-9(Hazardous Substances Data)

Upstream product

• 19451-11-7 cyclopropyliodide 
• 33577-99-0 2-ethynyl-benzoic acid methyl ester 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 6746-94-7 Cyclopropylacetylene 
• 610-94-6 2-bromobenzoic acid methyl ester 

Downstream Products

• 1420786-93-1 C₂₆H₂₈O₁₁ 
• 1420786-96-4 C₂₆H₂₈O₁₁ 
• 1038411-45-8 C₄₇H₄₈O₇ 
• 1492022-11-3 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl ortho-cyclopropylethynylbenzoate 
• 1038411-37-8 C₄₇H₄₈O₇ 
• 1219934-97-0 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-α-glucopyranosyl ortho-(hex-1-ynyl)benzoate 

Relevant articles and documents

Total Synthesis and Structural Revision of Mangrolide D

The unique 18-membered macrocyclic natural product mangrolide D was prepared in totally synthetic form. Key steps feature an Au-catalyzed glycosylation, aza-Michael addition, and LaLi3tris(binaphthoxide) catalyzed epoxidation. Detailed analysis

Green preparation method of 3-hydroxy isoindole-1-one compounds

The invention discloses a green preparation method of 3-hydroxy isoindole-1-one compounds, and belongs to the technical field of organic synthesis. The method comprises the following steps: adopting 2-alkynyl benzamide as a reaction substrate, adding a br

PhI(OCOCF3)2-Mediated Cyclization of o -(1-Alkynyl)benzamides: Metal-Free Synthesis of 3-Hydroxy-2,3-dihydroisoquinoline-1,4-dione

The synthesis of an undocumented skeleton of 3-hydroxy-2,3-dihydroisoquinoline-1,4-diones has been discovered and reported. The reaction consists of an intramolecular cyclization of o-(1-alkynyl)benzamides in MeCN/H2O, mediated by metal-free, h