(2E)-3-(1H-Imidazol-4-yl)acrylic acid

CAS

3465-72-3

Catalog Number

ACM3465723

Category

Other Products

Molecular Weight

138.124

Molecular Formula

C₆H₆N₂O₂

MSDS COA Spec Sheet

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Specification

Synonyms

(E)-urocanic acid; trans-Urocanic Acid; E-3-(4-Pyridyl)-1-phenylprop-2-en-1-on; (Z)-4-pyridalacetophenone; (E)-3-(1H-imidazol-4-yl)acrylic acid; E-3-(imidazol-4-yl)propenoic acid; 1-phenyl-3-(4-pyridinyl)-2-propen-1-one; 4-Imidazoleacrylic Acid; trans-4-i

IUPAC Name

(E)-3-(1H-imidazol-5-yl)prop-2-enoic acid

InChI Key

LOIYMIARKYCTBW-OWOJBTEDSA-N

Boiling Point

456.9ºC at 760mmHg

Flash Point

230.1ºC

Density

1.43g/cm³

Exact Mass

138.04300

H-Bond Acceptor

H-Bond Donor

Downstream Synthesis Route 1

3465-72-3

3718-04-5

Reference: [1] European Journal of Organic Chemistry, 2018, vol. 2018, # 1, p. 60 - 77
[2] Organic Mass Spectrometry, 1984, vol. 19, # 1, p. 16 - 22

Downstream Synthesis Route 2

3465-72-3

645-65-8
3034-50-2
1072-84-0

Reference: [1] Patent: EP1196129, 2005, B1, . Location in patent: Page/Page column 5; 14; 15; 22

Downstream Synthesis Route 3

3465-72-3

645-65-8
3034-50-2
1072-84-0
7699-35-6

Reference: [1] Patent: EP1196129, 2005, B1, . Location in patent: Page/Page column 4; 5; 7; 8; 21; 22

Downstream Synthesis Route 4

3465-72-3

3718-04-5

Reference: [1]European Journal of Organic Chemistry,2018,vol. 2018,p. 60 - 77
[2]Organic Mass Spectrometry,1984,vol. 19,p. 16 - 22

Downstream Synthesis Route 5

67-56-1
3465-72-3

54260-89-8

Reference: [1]Current Patent Assignee: SOUTHERN ILLINOIS UNIVERSITY - WO2018/209267, 2018, A2
Location in patent: Paragraph 0158; 0160
[2]Gupta, Preeti; Hameed, Shahul; Jain, Rahul
[European Journal of Medicinal Chemistry, 2004, vol. 39, # 9, p. 805 - 814]
[3]Sellier, Christian; Buschauer, Armin; Elz, Sigurd; Schunack, Walter
[Liebigs Annalen der Chemie, 1992, # 4, p. 317 - 324]
[4]Kimoto; Fujii; Cohen
[Journal of Organic Chemistry, 1984, vol. 49, # 6, p. 1060 - 1064]
[5]Wang, Yong-Gang; Morinaka, Brandon I.; Reyes, Jeremy Chris P.; Wolff, Jeremy J.; Romo, Daniel; Molinski, Tadeusz F.
[Journal of Natural Products, 2010, vol. 73, # 3, p. 428 - 434]

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

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