全部照片(1)
About This Item
經驗公式（希爾表示法）:
C3H5ClO
CAS號碼:
分子量：:
92.52
Beilstein:
1420784
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22
推薦產品
![1,8-二氮杂双环[5.4.0]十一碳-7-烯 98%](/deepweb/assets/sigmaaldrich/product/structures/120/564/5b373e23-1624-489c-8efb-692de0f96ffb/640/5b373e23-1624-489c-8efb-692de0f96ffb.png)
蒸汽密度
3.2 (vs air)
品質等級
蒸汽壓力
12.5 mmHg ( 20 °C)
化驗
98%
光學活性
[α]20/D +35°, c = 1 in methanol
光學純度
ee: 97% (GLC)
自燃溫度
1421 °F
expl. lim.
21 %
折射率
n20/D 1.438 (lit.)
bp
92-93 °C/360 mmHg (lit.)
密度
1.183 g/mL at 25 °C (lit.)
官能基
chloro
ether
SMILES 字串
ClC[C@@H]1CO1
InChI
1S/C3H5ClO/c4-1-3-2-5-3/h3H,1-2H2/t3-/m1/s1
InChI 密鑰
BRLQWZUYTZBJKN-GSVOUGTGSA-N
尋找類似的產品？ 前往 產品比較指南
應用
作为潜在的代谢调节剂，用以合成脂肪酸氧化抑制剂。
用于 Macquarimicins 的全合成和大环内酯 RK-397 的全合成。
用于对映选择性合成羟基异噁唑烷和 (+)-顺式-sylvaticin（一种有潜力的抗肿瘤剂）的手性结构单元。
法律資訊
经Sterling Pharma Solutions Limited许可，使用Jacobsen HKR技术制造。
訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
89.6 °F - closed cup
閃點（°C）
32 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Timothy J Donohoe et al.
Journal of the American Chemical Society, 128(42), 13704-13705 (2006-10-19)
The double oxidative cyclization of dienes is a viable procedure for making complex natural products containing cis-THF units. A double deprotection/double oxidative cyclization strategy using catalytic osmium tetroxide was used to construct the bisheterocyclic core of cis-sylvaticin and ultimately confirm
Ryosuke Munakata et al.
Journal of the American Chemical Society, 125(48), 14722-14723 (2003-12-04)
The first total synthesis of (+)-macquarimicin A (1), a novel inhibitor of neutral sphingomyelinase (N-SMase) with antiinflammatory activity, has been accomplished. The present work determined the absolute configuration of (+)-1 and revised the C(2)-C(3) geometry to be Z. The synthesis
Elfatih Elzein et al.
Bioorganic & medicinal chemistry letters, 14(4), 973-977 (2004-03-12)
We describe the synthesis of novel inhibitors of fatty acid oxidation as potential metabolic modulators for the treatment of stable angina. Replacement of the 2H-benzo[d]1,3-dioxolene ring system in our initial lead 3 with different benzthiazoles, benzoxazoles and introducing small alkyl
Tetrahedron Letters, 47, 7635-7635 (2006)
Svetlana A Burova et al.
Journal of the American Chemical Society, 126(8), 2495-2500 (2004-02-26)
The total synthesis of the natural product RK-397 is based on a new synthetic strategy for assembling polyacetate structures, by efficient cross-coupling of nucleophilic terminal alkyne modules with electrophilic epoxides bearing another alkyne at the opposite terminus. The natural product
我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.
聯絡技術服務