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2,2,3-Trimethyl-but-3-en-1-ol, also known as tert-amyl alcohol or 2,2,3-trimethyl-3-buten-1-ol, is an organic compound with the chemical formula C8H16O. It is a colorless liquid with a strong, pungent odor and is derived from the reduction of 2,2,3-trimethylbutanal. 2,2,3-trimethyl-but-3-en-1-ol is used as a solvent, a chemical intermediate, and a fragrance component in various applications, including the production of perfumes and flavorings. It is also known for its use in the synthesis of other chemicals and as a fuel additive. Due to its volatility and potential health effects, it is important to handle 2,2,3-trimethyl-but-3-en-1-ol with care, following proper safety guidelines.

3329-43-9

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3329-43-9 Usage

General Description

2,2,3-trimethyl-but-3-en-1-ol, also known as geraniol, is a naturally occurring chemical compound commonly found in essential oils such as rose, geranium, and citronella. It is a colorless liquid with a sweet, floral aroma, and is often used in perfumes and personal care products for its fragrance. Geraniol also has antimicrobial properties, making it a common ingredient in insect repellents and skincare products. Additionally, it has been studied for its potential therapeutic effects, including anti-inflammatory and antioxidant properties. However,

Check Digit Verification of cas no

The CAS Registry Mumber 3329-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3329-43:
(6*3)+(5*3)+(4*2)+(3*9)+(2*4)+(1*3)=79
79 % 10 = 9
So 3329-43-9 is a valid CAS Registry Number.

3329-43-9Relevant academic research and scientific papers

Fragmentierungsreaktionen an Carbonylverbindungen mit β-staendigen elektronegativen Substituenten, XXXIII 3-Oxatricyclo1,4>undec-4-en, ein stark gespannter Vierring-Enolether

Gerdes, Hero,Javeri, Shailaja,Marschall, Helga

, p. 1907 - 1920 (2007/10/02)

The behaviour of β-keto tosylates against nucleophiles has been investigated.The keto tosylate 6 underwent intramolecular cyclization with KOtBu in ether to produce exclusively the four-membered O-alkylated product 18 (the title compound).The substitution products 5 or 7 are obtained from 6 with NaOMe in methanol or KCN in DMSO, resp.Reaction of 6 with MeLi yielded the diol 13.The keto tosylate 31 reacted with MeLi analogously to form the diol 28, whereas with MeMgI a mixture of the Grob fragmentation product 33 and the alcohol 32 (via 28 by H2O elimination) was produced.Similarly keto tosylate 22b and MeMgI yielded the alcohol 27. - The non-enolizable keto tosylate 44 undergoes very slow reaction wih NaOH/MeOH to produce 41, 42, and 45 in low yield.

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