所有图片(1)
About This Item
线性分子式:
H2C=C(Cl)CH2OH
CAS号:
分子量:
92.52
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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等級
technical grade
化驗
90%
形狀
liquid
折射率
n20/D 1.459 (lit.)
bp
133-134 °C (lit.)
密度
1.162 g/mL at 25 °C (lit.)
SMILES 字串
OCC(Cl)=C
InChI
1S/C3H5ClO/c1-3(4)2-5/h5H,1-2H2
InChI 密鑰
OSCXYTRISGREIM-UHFFFAOYSA-N
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一般說明
据报道，2-氯-2-丙烯-1-醇会在193 nm处发生光离解以生成CH2CCH2OH自由基中间体。 2-氯-2-丙烯-1-醇是在1,2,3-三氯丙烷的碱介导反应过程中形成的主要产物。 据报道，2-氯-2-丙烯-1-醇可与三氯化磷反应生成亚磷酸酯，而与氯化磷反应生成磷酸酯。
應用
2-氯-2-丙烯-1-醇（2-氯丙烯醇）可以用作碳假单胞菌菌株生长的碳补充剂。 它可以用于制备2-（4-辛基苯基）-2-丙烯-1-醇。
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Flam. Liq. 3
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
129.2 °F - closed cup
閃點（°C）
54 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
其他客户在看
Arjun S Raman et al.
The Journal of chemical physics, 127(15), 154316-154316 (2007-10-24)
These velocity map imaging experiments characterize the photolytic generation of one of the two radical intermediates formed when OH reacts via an addition mechanism with allene. The CH2CCH2OH radical intermediate is generated photolytically from the photodissociation of 2-chloro-2-propen-1-ol at 193
Derivatives of phosphorus acids and 2-chloro-2-propen-1-ol.
Arbuzov BA, et al.
Russian Chemical Bulletin, 16(6), 1233-1238 (1967)
J J van der Waarde et al.
Applied and environmental microbiology, 59(2), 528-535 (1993-02-01)
Three Pseudomonas strains capable of utilizing 2-chloroallylalcohol (2-chloropropenol) as the sole carbon source for growth were isolated from soil. The fastest growth was observed with strain JD2, with a generation time of 3.6 h. Degradation of 2-chloroallylalcohol was accompanied by
Kinetic studies of the homogeneous abiotic reactions of several chlorinated aliphatic compounds in aqueous solution.
Pagan M, et al.
Applied Geochemistry, 13(6), 779-785 (1998)
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Journal of medicinal chemistry, 50(25), 6428-6435 (2007-11-13)
Compound 1 (FTY720, Fingolimod) represents a new generation of immunosuppressant that modulates lymphocyte trafficking by interacting with the S1P(1) receptor. Compound 1 also provides a template molecule for studying the molecular biology of S1P receptors and related enzymes (kinases and
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