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4-METHYL-3-PENTEN-1-OL

Product Name
4-METHYL-3-PENTEN-1-OL
CAS No.
763-89-3
Chemical Name
4-METHYL-3-PENTEN-1-OL
Synonyms
4-methyl-3-pentenol;4-METHYL-3-PENTEN-1-OL;4-methylpent-3-en-1-ol;3-Penten-1-ol, 4-methyl-;4-Methyl-3-penten-1-ol 97%
CBNumber
CB5380273
Molecular Formula
C6H12O
Formula Weight
100.16
MOL File
763-89-3.mol
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4-METHYL-3-PENTEN-1-OL Property

Melting point:
22.55°C (estimate)
Boiling point:
157 °C (lit.)
Density 
0.858 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.445(lit.)
Flash point:
146 °F
storage temp. 
2-8°C
pka
15.17±0.10(Predicted)
LogP
1.606 (est)
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Safety

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H227Combustible liquid

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
311200
Product name
4-Methyl-3-penten-1-ol
Purity
97%
Packaging
1g
Price
$477
Updated
2024/03/01
Crysdot
Product number
CD13004847
Product name
4-Methylpent-3-en-1-ol
Purity
95+%
Packaging
5g
Price
$662
Updated
2021/12/16
AHH
Product number
MT-18480
Product name
4-Methyl-3-penten-1-ol
Purity
97%
Packaging
5g
Price
$415
Updated
2021/12/16
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4-METHYL-3-PENTEN-1-OL Chemical Properties,Usage,Production

Uses

4-Methyl-3-penten-1-ol was used in the synthesis of tetrahydrofuro[3,2-c]benzothiopyran with a trans:cis ratio of 78:22.

Definition

ChEBI: 4-methylpent-3-en-1-ol is a homoallylic alcohol that is 2-methylpent-2-ene in which a hydrogen of the methyl group at position 5 has been replaced by a hydroxy group. It has a role as a plant metabolite. It is a homoallylic alcohol and a primary alcohol.

4-METHYL-3-PENTEN-1-OL Preparation Products And Raw materials

Raw materials

Preparation Products

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763-89-3, 4-METHYL-3-PENTEN-1-OLRelated Search:


  • 4-methyl-3-pentenol
  • 4-methylpent-3-en-1-ol
  • 4-METHYL-3-PENTEN-1-OL
  • 4-Methyl-3-penten-1-ol 97%
  • 3-Penten-1-ol, 4-methyl-
  • 763-89-3
  • CH32CCHCH2CH2OH
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  • Acyclic
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  • Chemical Synthesis
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