4-Ethynylbenzoic acid MedChemExpress (MCE)

Product Name	4-Ethynylbenzoic acid
Synonyms	RARECHEM AL BO 1500;P-ETHYNYLBENZOIC ACID;4-Ethynylbenzoic acid;p-Ethynylbenzoic Acid;4-ETHYNYL-BENZOIC ACID;4-Eethynylbenzoic acid;Benzoic acid, 4-ethynyl- (9CI)
CAS	10602-00-3
EINECS
Chemical Formula	C9H6O2
Molecular Weight	146.14
inchi	InChI=1/C9H6O2/c1-2-7-3-5-8(6-4-7)9(10)11/h1,3-6H,(H,10,11)
Package	10 mM * 1 mL;1 g;5 g;10 g;25 g
Price	Email to quote
Descriptions	4-Ethynylbenzoic acid 4-Ethynylbenzoic acid MedChemExpress (MCE) HY-W007533 10602-00-3 99.41% Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Room temperature in continental US Descriptions 4-Ethynylbenzoic acid 4-Ethynylbenzoic acid MedChemExpress (MCE) HY-W007533 10602-00-3 99.41% Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Room temperature in continental US may vary elsewhere. 4-Ethynylbenzoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 4-Ethynylbenzoic acid is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Click chemistry is used to describe the selective, modular, wide range and high-yield chemical reactions that allow rapid synthesis of new compounds through heteroatom linking (C-X-C). Bertozzi developed click chemistry in a new dimension —Bioorthogonal chemistry. It is defined as a rapid and selective reaction that does not interfere with biological processes under physiological conditions. Common reaction structures of click chemistry, such as Azide, Alkyne, DBCO, BCN, TCO and Tetrazine.? \| \| \| \| \| \| \| \| \| \|
Last Update	2025-04-01 14:45:47

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