205250-12-0

Basic information

• Product Name: Benzoic acid, 2-[(trimethylsilyl)ethynyl]-
• CAS NO: 205250-12-0
• Molecular Formula: C12H14O2Si
• Molecular Weight: 218.327
• Mol File: 205250-12-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[(trimethylsilyl)ethynyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[(trimethylsilyl)ethynyl]-(205250-12-0)
• EPA Substance Registry System: Benzoic acid, 2-[(trimethylsilyl)ethynyl]-(205250-12-0)

Safety Data

• Hazardous Substances Data: 205250-12-0(Hazardous Substances Data)

Upstream product

• 77123-58-1 2-[2-(trimethylsilyl)ethynyl]benzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 1066-54-2 trimethylsilylacetylene 
• 124-38-9 carbon dioxide 
• 38274-16-7 2-bromo-1-(trimethylsilylethynyl)benzene 

Downstream Products

• 1314659-70-5 4-(1-benzyl-1H-1,2,3-triazol-4-yl)-N,N-bis(pyridin-2-ylmethyl)benzamide 
• 1314659-68-1 4-ethynyl-N,N-bis(pyridin-2-ylmethyl)benzamide 
• 1171937-74-8 methyl 4-(1-benzyl-1H-1,2,3-triazol-4-yl)benzoate 

Relevant articles and documents

A Regio- and Stereoselective Carbonylative Approach to Alkyl (Z)-2-[3-Oxoisobenzofuran-1-(3H)-ylidene]acetates

The first example of the oxidative carbonylation of 2-ethynylbenzoic acid derivatives, leading to alkyl (Z)-2-[3-oxoisobenzofuran-1-(3H)-ylidene]acetates in a regio- and stereoselective manner, is reported. Under the catalytic action of PdI2 (2

An Efficient Stereospecific Preparation of (Z)-3-Methylidene-selenophthalides and (Z)-3-Methylidenetellurophthalides [1]

(Z)-3-Methylideneselenophthalides 5A and (Z)-3-methylidenetellurophthalides 5B were easily prepared by the regioselective and stereoselective reaction of 2-ethynylbenzoyl chlorides 3 with sodium hydroselenide and sodium hydrotelluride in good yields, resp