CAS
37517-26-3 Purity
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37517-26-3 Purity
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![6,7-Dimethoxy-N'-[2-(2-methoxyphenoxy)ethyl]-1,2,3,4-tetrahydroisoquinolin-2-ium-2-carboximidamide bromide](https://resource.alfa-chemistry.com/structure/37519-65-6.gif)
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Methyl malonyl chloride
CAS
37517-81-0
Catalog Number
ACM37517810
Category
Other Products
Molecular Weight
136.53
Molecular Formula
C4H5ClO3
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Specification
Synonyms
Methyl malonyl chloride, Methyl chloroformylacetate, Methyl 3-chloro-3-oxopropionate, 164011_ALDRICH, 63406_FLUKA, EINECS 253-540-6, CID123460, ZINC02170332, METHYL-3-CHLORO-3-OXOPROPIONATE, AI3-51039, ST5412135, TL8002758, Propanoic acid, 3-chloro-2-oxo-, methyl ester, 37517-81-0
IUPAC Name
methyl 3-chloro-3-oxopropanoate
Canonical SMILES
COC(=O)CC(=O)Cl
InChI Key
UTBCRHAMJFMIIR-UHFFFAOYSA-N
Boiling Point
57-59ºC (12 mmHg)
Flash Point
80ºC
Density
1.273
Appearance
Clear light yellow to yellow liquid
EC Number
253-540-6
Exact Mass
135.99300
Hazard Statements
C:Corrosive;
H-Bond Acceptor
3
H-Bond Donor
0
Packing Group
II
Safety Description
S26-S36/37/39-S45
Stability
Stable under normal temperatures and pressures. May decompose on exposure to moist air or water.
WGK Germany
3
Upstream Synthesis Route 1
- 16695-14-0
- 37517-81-0
Reference: [1] Tetrahedron, 1993, vol. 49, # 23, p. 5133 - 5146
[2] Journal of Medicinal Chemistry, 1985, vol. 28, # 5, p. 559 - 586
[3] Patent: US5912349, 1999, A,
[4] Patent: CN106083804, 2016, A, . Location in patent: Paragraph 0012
Upstream Synthesis Route 2
- 38330-80-2
- 37517-81-0
Reference: [1] Heterocycles, 1991, vol. 32, # 2, p. 245 - 251
[2] Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1982, vol. 36, # 7, p. 435 - 442
[3] Analytical Chemistry, 1995, vol. 67, # 2, p. 324 - 334
[4] Journal of Agricultural and Food Chemistry, 1995, vol. 43, # 4, p. 1052 - 1056
[5] Angewandte Chemie - International Edition, 2008, vol. 47, # 52, p. 10155 - 10158
Downstream Synthesis Route 1
- 37517-81-0
- 925-90-6
- 30414-53-0
Reference: [1] Organic Letters, 2008, vol. 10, # 22, p. 5269 - 5271
Downstream Synthesis Route 2
- 37517-81-0
- 49755-94-4
- 141509-99-1
Reference: [1]Padwa, Albert; Kinder, Frederic R.; Nadler, William R.; Zhi, Lin
[Heterocycles, 1993, vol. 35, # 1, p. 367 - 383]
Downstream Synthesis Route 3
- 37517-81-0
- 35309-35-4
- 196882-11-8
Reference: [1]Sano; Toda; Shoda; Yamamoto; Ando; Isobe; Hosoi; Tsuda
[Chemical and Pharmaceutical Bulletin, 1992, vol. 40, # 12, p. 3145 - 3156]
Downstream Synthesis Route 4
- 37517-81-0
- 22049-95-2
- 196881-98-8
Reference: [1]Andrisano; Di Bella; Ferrari; Raffa; Baggio
[Farmaco, Edizione Scientifica, 1981, vol. 36, # 11, p. 905 - 915]
* For details of the synthesis route, please refer to the original source to ensure accuracy.
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