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Merck
CN

167304

碘丁烷

99%, contains copper as stabilizer

别名:

丁基碘

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线性分子式:
CH3(CH2)3I
化学文摘社编号:
分子量:
184.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1420755
Assay:
99%
Form:
liquid
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产品名称

碘丁烷, 99%, contains copper as stabilizer

InChI

1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3

SMILES string

CCCCI

InChI key

KMGBZBJJOKUPIA-UHFFFAOYSA-N

vapor density

~5 (vs air)

assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.498 (lit.)

bp

130-131 °C (lit.)

mp

−103 °C (lit.)

solubility

alcohol: soluble
diethyl ether: soluble
water: insoluble

density

1.617 g/mL at 25 °C (lit.)

functional group

alkyl halide
iodo

Quality Level

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Application

1-碘丁烷用于合成:
  • S -烷基化 5-(2-,3-和 4-甲氧基苯基)-4 H -1,2,4-三唑-3-硫醇
  • 5-(2-,3-和 4-甲氧基苯基)-4-苯基-4 H -1,2,4-三唑-3-硫醇
  • 在乙酸乙酯中与 1-甲基吡咯烷反应的 N -丁基- N -甲基吡咯并 (三氟甲磺酰基)酰亚胺

General description

通过程序升温脱附和反射-吸收红外光谱研究了1-碘丁烷在洁净、含氢和氘Pt(111)单晶表面的热化学。.

1-碘丁烷是一种烷基卤化物,在SN2亲核反应中用作亲电体。

pictograms

FlameSkull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Inhalation - Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

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Recent developments in the ENEA lithium metal battery project.
Shin J-H, et al.
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The journal of physical chemistry. B, 109(7), 2745-2753 (2006-07-21)
The thermal chemistry of a number of C4 hydrocarbons (1,3-butadiene, 1-bromo-3-butene, 1-bromo-2-butene, trans-2-butene, cis-2-butene, 1-butene, 2-iodobutane, 1-iodobutane, and butane) was investigated on clean and hydrogen- and deuterium-predosed Pt(111) single-crystal surfaces by temperature-programmed desorption and reflection-absorption infrared spectroscopy. A combination of
L Labanauskas et al.
Farmaco (Societa chimica italiana : 1989), 59(4), 255-259 (2004-04-15)
New S-alkylated 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiols (5a-c, 6a-c) and 5-(2-,3- and 4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiols (7a-c, 8a-c, 9a-c) were synthesized by the alkylation of 3-(2-,3- and 4-methoxyphenyl)-4,5-dihydro-1H-1,2,4-triazole-5-thiones (3a-c) or 3-(2-,3- and 4-methoxyphenyl)-4-phenyl-4,5-dihydro-1H-1,2,4-triazole-5-thiones (4a-c) with 1-iodobutane or 1-(1,3-benzodioxol-5-yl)-2-bromo-1-ethanone, 2-bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-ethanone and 2-bromo-1-(3,4-dihydro-2H-1,5-benzodioxepin-7-yl)-1-ethanone. Compounds 3a-c and 4a-c

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