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110701

Sigma-Aldrich

4,4-Dimethyl-1-pentene

99%

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About This Item

Linear Formula:
CH2=CHCH2C(CH3)3
CAS Number:
762-62-9
Molecular Weight:
98.19
Beilstein/REAXYS Number:
1731848
EC Number:
212-101-9
MDL number:
MFCD00026337
UNSPSC Code:
12352100
PubChem Substance ID:
24847000
NACRES:
NA.22
Pricing and availability is not currently available.

vapor pressure

231 mmHg ( 37.7 °C)

assay

99%

refractive index

n20/D 1.392 (lit.)

bp

72 °C (lit.)

density

0.683 g/mL at 25 °C (lit.)

functional group

allyl

SMILES string

CC(C)(C)CC=C

InChI

1S/C7H14/c1-5-6-7(2,3)4/h5H,1,6H2,2-4H3

InChI key

KLCNJIQZXOQYTE-UHFFFAOYSA-N

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1 of 4

This Item
136875443018406082
4,4-Dimethyl-1-pentene 99%

110701

4,4-Dimethyl-1-pentene

4,4-Dimethyl-2-pentanone 99%

136875

4,4-Dimethyl-2-pentanone

2,4,4-Trimethyl-1-pentene 96%

443018

2,4,4-Trimethyl-1-pentene

2,3,4-Trimethyl-2-pentene 96%

406082

2,3,4-Trimethyl-2-pentene

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

refractive index

n20/D 1.392 (lit.)

refractive index

n20/D 1.404 (lit.)

refractive index

n20/D 1.408 (lit.)

refractive index

n20/D 1.428 (lit.)

density

0.683 g/mL at 25 °C (lit.)

density

0.809 g/mL at 25 °C (lit.)

density

0.708 g/mL at 25 °C (lit.)

density

0.743 g/mL at 25 °C (lit.)

bp

72 °C (lit.)

bp

125-130 °C (lit.)

bp

101-102 °C (lit.)

bp

116 °C (lit.)

vapor pressure

231 mmHg ( 37.7 °C)

vapor pressure

-

vapor pressure

83 mmHg ( 37.7 °C)

vapor pressure

-

General description

4,4-Dimethyl-1-pentene is obtained by the S(N)2′ attack of the organolithium on allyl ether[1].

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

hcodes

H225,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

10.4 °F - closed cup

flash_point_c

-12 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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    Certificates of Analysis (COA)

    Lot/Batch Number
    MKBJ0066V
    02514DJ
    12209ED
    08321KS
    07025LA

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    Bailey et al.
    Organic letters, 2(4), 489-491 (2000-05-18)
    [reaction: see text] Allylic ethers are converted to the corresponding alcohol or phenol in virtually quantitative yield at temperatures below ambient simply by stirring a hydrocarbon solution of the ether with 1 molar equiv of tert-butyllithium. The reaction, which produces

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