Structure

Ethyl 2-amino-4-methyl-1,3-oxazole-5-carboxylate 95+%

CAS
79221-15-1
Catalog Number
ACM79221151
Category
Other Products
Molecular Weight
170.17
Molecular Formula
C7H10N2O3

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  • Product Description
  • Case Study
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Specification

Synonyms
79221-15-1, Ethyl 2-amino-4-methyloxazole-5-carboxylate, ethyl 2-amino-4-methyl-1,3-oxazole-5-carboxylate, 2-Amino-5-(ethoxycarbonyl)-4-methyl-1,3-oxazole, ACMC-209pgn, SureCN781841, ethylaminomethyloxazolecarboxylate, CTK5E6597, ANW-37269, AKOS006283535, AB49222, AG-H-17944, MCULE-4174769346, RP10488, AK-92703, BD230609, KB-50857, Ethyl-2-amino-4-methyloxazole-5-carboxylate, FT-0682908, EN300-75938
IUPAC Name
ethyl 2-amino-4-methyl-1,3-oxazole-5-carboxylate
SMILES
CCOC(=O)C1=C(N=C(O1)N)C
InChI Key
LACXTUNIUGNJDW-UHFFFAOYSA-N
Exact Mass
170.06900
H-Bond Acceptor
5
H-Bond Donor
1

Upstream Synthesis Route 1

  • 141-97-9
  • 57-13-6
  • 79221-15-1

Reference: [1] Patent: WO2010/13222, 2010, A1, . Location in patent: Page/Page column 67

Upstream Synthesis Route 2

  • 57-13-6
  • 609-15-4
  • 79221-15-1

Reference: [1] Indian Journal of Heterocyclic Chemistry, 2011, vol. 21, # 1, p. 13 - 18
[2] Patent: WO2015/193846, , A1, . Location in patent: Page/Page column 42; 43[2] Patent: , 2015, , . Location in patent: Page/Page column 42; 43

Upstream Synthesis Route 3

  • 141-97-9
  • 57-13-6
  • 79221-15-1

Reference: [1]Patent: WO2010/13222,2010,A1 .Location in patent: Page/Page column 67

Downstream Synthesis Route 1

  • 79221-15-1
  • 106-51-4
  • 79221-11-7

Reference: [1]Journal fur praktische Chemie (Leipzig 1954),1981,vol. 323,p. 516 - 520

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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