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Detail of "26367-48-6"

  • CAS Number:
  • 26367-48-6
  • Name:
  • 2-Butenoic acid,4-chloro-4-oxo-, ethyl ester, (2E)-

  • Superlist Name:
  • 3-Chlorocarbonylacrylic acid ethyl ester
  • Molecular Structure:
  • Formula:
  • C6H7ClO3
  • Molecular Weight:
  • 162.57
  • Synonyms:
  • Acrylic acid, 3-(chloroformyl)-,ethyl ester, (E)- (8CI);Ethyl trans-3-chloroformylacrylate;Fumaric acid chlorideethyl ester;Ethylfumaryl chloride;Fumaric acid chloride monoethyl ester;Fumaric acid ethyl ester chloride;trans-b-(Ethoxycarbonyl)acryloylchloride;Fumaric acid chloridemonomethyl ester;(E)-4-Chloro-4-oxo-2-butenoic acid ethyl ester;2-Butenoicacid, 4-chloro-4-oxo-, ethyl ester, (E)-;
  • Density:
  • 1.221 g/cm3
  • Boiling Point:
  • 217.704 °C at 760 mmHg
  • Flash Point:
  • 92.72 °C

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CAS No.26367-48-6 3-Chlorocarbonylacrylic acid ethyl ester

3-Chlorocarbonylacrylic acid ethyl ester industrial chemicals 3-Chlorocarbonylacrylic acid ethyl ester Molecular Formula C6H7ClO3 Molecular Weight 162.57 Density 1.220 Boiling point 218 oC Flash point 93 oC

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CAS No.26367-48-6 3-Chlorocarbonylacrylic acid ethyl ester

Supplier:Sarchem Laboratories, Inc. [ United States]

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CAS No.26367-48-6 3-Chlorocarbonylacrylic acid ethyl ester

3-Chlorocarbonylacrylic acid ethyl ester

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CAS No.26367-48-6 3-Chlorocarbonylacrylic acid ethyl ester

Supplier:Shanghai Eybridge Chemical Technology Co., Ltd [ China (Mainland)]

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CAS No.26367-48-6 3-Chlorocarbonylacrylic acid ethyl ester

Supplier:Jiangxi Sanjiang Fine Chemicals Co., Ltd. [ China (Mainland)]

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Reference

Ethyl 2',5'-dichloro-4'-thiocyanatofumaranilate
Ethyl 2',5'-dichloro-4'-thiocyanatofumaranilate. Pelosi, Stanford S., Jr. (Morton-Norwich Products, Inc., USA). U. 26367-48-6 and 772-12-3 are cas registry numbers. These chemicals are also mentioned in this article.S. US 4002659 11 Jan 1977, 2 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: C07C161-02. NCL: 260454000. APPLICATION: US 76-649584 16 Jan 1976. DOCUMENT TYPE: Patent CA Section: 25 (Noncondensed Aromatic Compounds) Section cross-reference(s): 5 (E)-I was prepd. by treatment of 2,5,4-Cl2(NCS)C6H2NH2 (II) with Et fumaroyl chloride (III) in acetone contg. K2CO3. (E)-I has antibacterial activity (no data). For example, a 60% yield of (E)-I was obtained by refluxing for 5 h approx. equimolar amts. of II and III in acetone contg. K2CO3 and then allowing to stand overnight. .
Can an aromatic ring alter the reactions of a nearby unsaturated imide? A study of the rate and selectivity of nitrile oxide cycloaddition reactions of acryloyl derivatives of the Rebek imide benzoxazole
Can an aromatic ring alter the reactions of a nearby unsaturated imide? A study of the rate and selectivity of nitrile oxide cycloaddition reactions of acryloyl derivatives of the Rebek imide benzoxazole. Curran, Dennis P.; Yoon, Moon-Hwan (Dep. of Chemistry, Univ. of Pittsburgh, Pittsburgh, PA 15260, USA). Tetrahedron, 53(6), 1971-1982 (English) 1997 Elsevier.Several reagents such as 188106-62-9 is used here. CODEN: TETRAB. ISSN: 0040-4020. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) Cycloaddns. of acryloyl derivs. of the Rebek imide benzoxazole (I; R = acryloyl, methacryloyl, crotonoyl, cinnamoyl, fumaroyl, 2,4-pentadienoyl) are extraordinarily stereoselective, but have rates and regioselectivities that otherwise parallel those of a simple achiral model. It appears that the benzoxazole rings of these compds. completely shields the inner face of the nearby alkene, but has no measurable effect on the rate of reactions on the outer face. .
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