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CAS Number: 19367-38-5
(E)-methyl 3-(4-hydroxyphenyl)acrylate

Structure

(E)-methyl 3-(4-hydroxyphenyl)acrylate
Name: (E)-methyl 3-(4-hydroxyphenyl)acrylate
Synonyms:
General Information
Product Number: 19367385

CAS Registry Number: 19367-38-5

Name:

2-​Propenoic acid, 3-​(4-​hydroxyphenyl)​-​, methyl ester, (2E)​-
2-​Propenoic acid, 3-​(4-​hydroxyphenyl)​-​, methyl ester, (E)​-; Cinnamic acid, p-​hydroxy-​, methyl ester, (E)​- (8CI); (E)​-​4-​Hydroxycinnamic acid methyl ester; (E)​-​Methyl p-​hydroxycinnamate; Methyl (E)​-​3-​(4-​hydroxyphenyl)​-​2-​propenoate; Methyl (E)​-​4-​hydroxycinnamate; Methyl (E)​-​p-​coumarate; Methyl (E)​-​p-​hydroxy-​cinnamate; Methyl (E)​-​p-​hydroxycinnamate; Methyl p-​hydroxy-​(E)​cinnamate; Methyl p-​hydroxy-​trans-​cinnamate; Methyl trans-​4-​hydroxycinnamate; Methyl trans-​p-​coumarate; trans-​Methyl p-​hydroxycinnamate; trans-​p-​Coumaric acid methyl ester 

 

Chemical Formula: C10H10O3
Exact Mass: 178.06
Molecular Weight: 178.18
m/z: 178.06 (100.0%), 179.07 (11.0%), 180.07 (1.2%)
Elemental Analysis: C, 67.41; H, 5.66; O, 26.94

 

InChI: InChI=1S/C10H10O3/c1-13-10(12)7-4-8-2-5-9(11)6-3-8/h2-7,11H,1H3/b7-4+
InChIKey: NITWSHWHQAQBAW-QPJJXVBHSA-N
Canonical SMILES : COC(=O)C=CC1=CC=C(C=C1)O
Isomeric SMILES: COC(=O)/C=C/C1=CC=C(C=C1)O

 

Thermal Properties Value Condition Note
Melting Point 140-141 °C   (15)CAS
Melting Point 139-140 °C   (10)CAS
Melting Point 138-140 °C   (12)CAS
Melting Point 137-139 °C   (6)CAS
Melting Point 136-138 °C   (13)CAS
Melting Point 136-137 °C   (16)CAS

Specification

98%

References
  1. (1) ACD: Spectral data were obtained from Advanced Chemistry Development, Inc.
  2. (2) Speranza, Giovanna; Journal of Natural Products 1988, V51(3), P588-90 CAPLUS
  3. (3) Silva, A. M. S.; Journal of Molecular Structure 2001, V595(1-3), P1-6 CAPLUS
  4. (4) El-Batta, Amer; Journal of Organic Chemistry 2007, V72(14), P5244-5259 CAPLUS
  5. (5) Patel, Chirag K.; Letters in Drug Design & Discovery 2004, V1(1), P35-44 CAPLUS
  6. (6) Duque Estrada, Gizelda O.; Catalysis Communications 2008, V9(8), P1734-1738 CAPLUS
  7. (7) Schmidt, Bernd; Advanced Synthesis & Catalysis 2010, V352(14+15), P2463-2473 CAPLUS
  8. (8) Dambacher, Jesse; Tetrahedron Letters 2005, V46(26), P4473-4477 CAPLUS
  9. (9) Yao, Chengfu; Catalysis Communications 2009, V10(7), P1099-1102 CAPLUS
  10. (10) Chiang, Yi-Ming; Journal of the Chinese Chemical Society (Taipei, Taiwan) 2003, V50(1), P161-166 CAPLUS
  11. (11) Akita, Hiroyuki; Journal of Molecular Catalysis B: Enzymatic 2006, V40(1-2), P8-15 CAPLUS
  12. (12) Venkateswarlu, Somepalli; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry 2006, V45B(1), P252-257 CAPLUS
  13. (13) Jiao, Jie; Journal of Enzyme Inhibition and Medicinal Chemistry 2010, V25(1), P132-138 CAPLUS
  14. (14) Narsaiah, A. Venkat; Synthetic Communications 2011, V41(11), P1603-1608 CAPLUS
  15. (15) Singh, Pradeep Pratap; Synthetic Communications 2008, V38(6), P928-936 CAPLUS
  16. (16) Burmaoglu, Serdar; Synthetic Communications 2009, V39(9), P1549-1562 CAPLUS
  17. (17) Quitschau, Melanie; European Journal of Organic Chemistry 2008, (30), P5117-5124, S5117/1-S5117/9 CAPLUS
  18. (18) Junek, Richard; European Journal of Medicinal Chemistry 2009, V44(1), P332-344 CAPLUS
  19. (19) Menon, Sanjay R.; Journal of Natural Products 1999, V62(1), P102-106 CAPLUS
  20. (20) Ueda, Rie; Journal of the American Chemical Society 2009, V131(48), P17536-17537 CAPLUS
  21. (21) Vengris, Mikas; Journal of Physical Chemistry B 2005, V109(9), P4197-4208 CAPLUS
  22. (22) Galland, Stephanie; Organic & Biomolecular Chemistry 2008, V6(22), P4253-4260 CAPLUS
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