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139130

Sigma-Aldrich

2-氯丙酸甲酯

97%

同義詞:

(±)-2-氯丙酸甲酯

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About This Item

線性公式:
CH3CHClCOOCH3
CAS號碼:
分子量::
122.55
Beilstein:
1421535
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

蒸汽密度

4.22 (vs air)

蒸汽壓力

5.25 mmHg ( 20 °C)

化驗

97%

expl. lim.

19 %

折射率

n20/D 1.417 (lit.)

bp

132-133 °C (lit.)

密度

1.075 g/mL at 25 °C (lit.)

SMILES 字串

COC(=O)C(C)Cl

InChI

1S/C4H7ClO2/c1-3(5)4(6)7-2/h3H,1-2H3

InChI 密鑰

JLEJCNOTNLZCHQ-UHFFFAOYSA-N

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一般說明

Methyl 2-chloropropionate is the initiating/catalyst system during the atom transfer radical polymerization of N,N-dimethylacrylamide, N-isopropylacrylamide and N-vinylpyrrolidone.

應用

Methyl 2-chloropropionate was used as initiator during the synthesis of acrylamide homopolymers and acrylamide-N-isopropylacrylamide block copolymers.

象形圖

FlameExclamation mark

訊號詞

Warning

危險分類

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - 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 1

閃點(°F)

100.4 °F - closed cup

閃點(°C)

38 °C - closed cup

個人防護裝備

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


分析證明 (COA)

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Thermal response of narrow-disperse poly (N-isopropylacrylamide) prepared by atom transfer radical polymerization.
Xia Y, et al.
Macromolecules, 38(14), 5937-5943 (2005)
Acrylamide Homopolymers and Acrylamide-N-Isopropylacrylamide Block Copolymers by Atomic Transfer Radical Polymerization in Water.
Wever DAZ, et al.
Macromolecules, 45(10), 4040-4045 (2012)
A I Gurova et al.
Gigiena truda i professional'nye zabolevaniia, (5)(5), 36-38 (1992-01-01)
Reports of MACs for carboxylic acid derivatives as sodium methoxyacetate (SMOA), methyl chlorpropionate (MCP) and acetoacetic ether (AAE). SMOA shows low toxicity, no cumulation and specific action MCP demonstrates moderate toxicity, low cumulation no specific action in concentrations close to
Controllable synthesis of poly (N-vinylpyrrolidone) and its block copolymers by atom transfer radical polymerization.
Lu X, et al.
Polymer, 48(10), 2835-2842 (2007)
J L Rakels et al.
Enzyme and microbial technology, 15(12), 1051-1056 (1993-12-01)
The enantiomeric ratio (E) is commonly used to characterize the enantioselectivity in enzyme-catalyzed kinetic resolution. In this paper this parameter is directly derived from the enantiomeric excess of substrate and product. This is formally more correct than using Chen's equation

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