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Key Documents

393665

Sigma-Aldrich

1,1-二溴-2,2-二(氯甲基)环丙烷

90%, technical grade

同義詞:

1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane

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About This Item

線性公式:
Br2C3H2(CH2Cl)2
CAS號碼:
分子量::
296.82
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

technical grade

品質等級

化驗

90%

形狀

solid

mp

48-50 °C (lit.)

官能基

bromo
chloro

SMILES 字串

ClCC1(CCl)CC1(Br)Br

InChI

1S/C5H6Br2Cl2/c6-5(7)1-4(5,2-8)3-9/h1-3H2

InChI 密鑰

RCRVZCIUKQNOIS-UHFFFAOYSA-N

一般說明

1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane is a halogenated cyclopropane derivative. It has been reported to be synthesized from 3-chloro-2-(chloromethyl)-1-propene. It is formed as an intermediate during the synthesis of [1.1.1]propellane by Szeimies method.

應用

1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane may be used as a starting material in the synthesis of [1.1.1]-propellane and ((3-ethynylbicyclo[1.1.1]pentan-1-yl)ethynyl)trimethylsilane.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Concerning the synthesis of [1.1. 1] propellane.
Belzner J, et al.
Chemische Berichte, 122(2), 397-398 (1989)
Cyprien Lemouchi et al.
Journal of the American Chemical Society, 135(25), 9366-9376 (2013-06-04)
The rod-like molecule bis((4-(4-pyridyl)ethynyl)bicyclo[2.2.2]oct-1-yl)buta-1,3-diyne, 1, contains two 1,4-bis(ethynyl)bicyclo[2.2.2]octane (BCO) chiral rotators linked by a diyne fragment and self-assembles in a one-dimensional, monoclinic C2/c centrosymmetric structure where two equilibrium positions with large occupancy imbalance (88% versus 12%) are identified on a
Improved Preparations of 3-Chloro-2-(chloromethyl)-1-propene and 1, 1-Dibromo-2, 2-bis (chloromethyl) cyclopropane: Intermediates in the Synthesis of [1.1. 1] Propellane.
Lynch KM and Dailey WP
The Journal of Organic Chemistry, 60(14), 4666-4668 (1995)
[1.1. 1] Propellane: Reaction with Singlet Dihalocarbene.
Lee WB, et al.
Bull. Korean Chem. Soc., 19(3), 367-369 (1998)

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