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Key Documents

125903

Sigma-Aldrich

1,3-二溴丙烷

ReagentPlus®, 99%

同義詞:

三亚甲基二溴

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About This Item

線性公式:
Br(CH2)3Br
CAS號碼:
分子量::
201.89
Beilstein:
635662
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.21

蒸汽密度

7 (vs air)

品質等級

產品線

ReagentPlus®

化驗

99%

形狀

liquid

折射率

n20/D 1.524 (lit.)

bp

167 °C (lit.)

mp

−34 °C (lit.)

密度

1.989 g/mL at 25 °C (lit.)

SMILES 字串

BrCCCBr

InChI

1S/C3H6Br2/c4-2-1-3-5/h1-3H2

InChI 密鑰

VEFLKXRACNJHOV-UHFFFAOYSA-N

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一般說明

1,3-二溴丙烷是一种二卤代丙烷。在碳电极表面的聚合物膜中,它分别被电生液相镍 (I) 手性和镍 (I) 手性催化还原生成环丙烷和丙烯。

應用

1,3-二溴丙烷可用于制备手性孪生双阳离子离子液体 和 1,3-双(1-7′-氯-4-喹啉基-4-哌嗪基)丙烷。3

法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Liq. 3 - Skin Irrit. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

129.2 °F - closed cup

閃點(°C)

54 °C - closed cup

個人防護裝備

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


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Catalytic reduction of α,ω-dihaloalkanes with nickel (I) salen as a homogeneous-phase and polymer-bound mediator.
Dahm CE and Peters DG.
Journal of Electroanalytical Chemistry, 406(1), 119-129 (1996)
Synthesis of Chiral Geminal Dicationic Ionic Liquid from Amino Acids.
Yin A, et al.
Asian Journal of Chemistry, 25(12), 6721-6721 (2013)
E E Badr et al.
Journal of oleo science, 59(12), 647-652 (2010-11-26)
A fatty hydrazide based cationic gemini surfactants, 1,3-bis (N'-acyl-N,N-dimethylhydrazinium) propane dibromide which possess hydrolyzable amido moieties in the lipophilic portions, were prepared by reacting 1,3-bromopropane with N,N-dimethyl fatty hydrazide. The surface properties were explained and discussed based on the effect
A Witkowski et al.
The Journal of biological chemistry, 267(26), 18488-18492 (1992-09-15)
Thioesterase II is a 29-kDa monomer which, in certain specialized tissues, acts as a chain terminator in fatty acid synthesis by hydrolyzing medium-chain fatty acids from the fatty acid synthase. As with serine proteases, hydrolysis appears to involve acylation of
S P James et al.
Toxicology letters, 8(1-2), 7-15 (1981-04-01)
Oral administration of 1,3-dibromopropane (2 mmol/kg) to rats resulted in a marked decrease in the level of hepatic glutathione (GSH). Sulphur-containing [14C]-metabolites were excreted in the bile of rats dose with 1,3-bromo[14C]propane and were subjected to enterohepatic cycling. After an

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