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Merck

10905

Sigma-Aldrich

氯丙酮

produced by Wacker Chemie AG, Burghausen, Germany, ≥96.0% (GC)

别名:

MCA, 1-氯-2-丙酮, 氯-2-丙酮

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About This Item

线性分子式:
ClCH2COCH3
CAS号:
分子量:
92.52
Beilstein:
605369
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

produced by Wacker Chemie AG, Burghausen, Germany

化驗

≥96.0% (GC)

包含

~0.1% Drapex 39 as stabilizer

折射率

n20/D 1.432 (lit.)

bp

120 °C (lit.)

溶解度

H2O: soluble 10 parts
alcohol: miscible
chloroform: miscible
diethyl ether: miscible

密度

1.162 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CC(=O)CCl

InChI

1S/C3H5ClO/c1-3(5)2-4/h2H2,1H3

InChI 密鑰

BULLHNJGPPOUOX-UHFFFAOYSA-N

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一般說明

氯丙酮与L-脯氨酸酰胺催化的 4-硝基苯甲醛发生直接羟醛反应。它与羧酸反应形成酯衍生物

應用

氯丙酮用于氯丙酮的微生物不对称还原合成手性 1,2-环氧丙烷。它用于通过气相色谱分析酸。它还用于和 1-((3-(萘并[2,1-b]呋喃-2-基)-1-苯基-1H-吡唑-4-基)亚甲基)-2-苯腙反应合成甲基噻唑衍生物

其他說明

可根据要求提供批量价格

訊號詞

Danger

危險分類

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

95.0 °F - closed cup

閃點(°C)

35 °C - closed cup

個人防護裝備

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


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分析证书(COA)

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Analysis of carboxylic acids by gas chromatography. Derivatisation using chloroacetone.
McCalley DV, et al.
Chromatographia, 18(6), 309-312 (1984)
Synthesis of optically pure 1, 2-epoxypropane by microbial asymmetric reduction of chloroacetone.
Weijers CAGM, et al.
Applied Microbiology and Biotechnology, 38(3), 297-300 (1992)
Ashraf H F Abd El-Wahab et al.
Molecules (Basel, Switzerland), 16(1), 307-318 (2011-01-27)
Vilsmeier formylation of 2-(1-phenylhydrazonoethyl)naphtho[2,1-b]furan (2) gave 3-naphtho[2,1-b]furan-2-yl-1-phenyl-1H-pyrazole-4-carbaldehyde (3), which was reacted with C- and N-nucleophiles to afford naphthofuranpyrazol derivatives 4-8. Treatment of 2-[(3-(naphtho[2,1-b]furan-2-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-malononitrile (4a) with reactants having active hydrogen and Et₃N gave the corresponding pyrazoline, pyran and chromene addition product
L-Proline amide-catalyzed direct asymmetric aldol reaction of aldehydes with chloroacetone.
He L, et al.
Tetrahedron, 62(2), 346-351 (2006)
Dose-response relationships for mutations induced in E. coli by some model compounds. With an addendum: Reaction kinetics in water of chloroethylene oxide, chloroacetaldehyde, and chloroacetone.
S Hussain et al.
Hereditas, 101(1), 57-68 (1984-01-01)

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