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4-ETHYLCINNAMIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28784-98-7 Structure
  • Basic information

    1. Product Name: 4-ETHYLCINNAMIC ACID
    2. Synonyms: (E)-3-(4-ETHYLPHENYL)-2-PROPENOIC ACID;3-(4-ETHYL-PHENYL)-ACRYLIC ACID;3-(4-ETHYLPHENYL)-2-PROPENOIC ACID;(2E)-3-(4-ETHYLPHENYL)ACRYLIC ACID;4-ETHYLCINNAMIC ACID;RARECHEM BK HC T310;(E)-3-(4-ethylphenyl)prop-2-enoic acid;10R-0618
    3. CAS NO:28784-98-7
    4. Molecular Formula: C11H12O2
    5. Molecular Weight: 176.21
    6. EINECS: N/A
    7. Product Categories: Acids & Esters
    8. Mol File: 28784-98-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 312.5°C at 760 mmHg
    3. Flash Point: 217.3°C
    4. Appearance: /
    5. Density: 1.116g/cm3
    6. Vapor Pressure: 0.000225mmHg at 25°C
    7. Refractive Index: 1.589
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-ETHYLCINNAMIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-ETHYLCINNAMIC ACID(28784-98-7)
    12. EPA Substance Registry System: 4-ETHYLCINNAMIC ACID(28784-98-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 28784-98-7(Hazardous Substances Data)

28784-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28784-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,8 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28784-98:
(7*2)+(6*8)+(5*7)+(4*8)+(3*4)+(2*9)+(1*8)=167
167 % 10 = 7
So 28784-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O2/c1-2-9-3-5-10(6-4-9)7-8-11(12)13/h3-8H,2H2,1H3,(H,12,13)

28784-98-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-ethylphenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 4-Ethylcinnamic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28784-98-7 SDS

28784-98-7Relevant articles and documents

Cu/Fe-Cocatalyzed Formation of β-Ketophosphonates by a Domino Knoevenagel-Decarboxylation-Oxyphosphorylation Sequence from Aromatic Aldehydes and H-Phosphonates

Zhou, Mingxin,Zhou, Yao,Song, Qiuling

supporting information, p. 10654 - 10658 (2015/07/20)

A domino Knoevenagel-decarboxylation-alkene difunctionalization sequence has been developed for the conversion of benzaldehydes into β-ketophosphonates, catalyzed by a cooperative Cu/Fe system, whereby CP and CO bonds are formed simultaneously in a one-pot reaction. The reaction proceeds in good yields and with a broad substrate scope and environmentally benign conditions.

Improved synthesis of natural ester sintenin and its analogues via Wittig reaction

Sharma, Mukul,Rajesh, U. Chinna,Rawat, Diwan S.

, p. 1853 - 1860 (2014/01/17)

The synthesis of a cytotoxic natural ester sintenin (7a) and twenty eight of its analogues including nitrogen-containing heterocyclic indole moiety (7b-7t), saturated (10a-10d) and unsaturated (10e-10h) amides were carried out by convenient route via one-pot Wittig reaction in aqueous medium with improved yield. A systematic structure activity relationship of sintenin ester was designed by chemically modified derivatives in order to get better cytotoxicity.

Synthesis and anticancer activity of 13-membered cyclic enediynes

Sharma, Mukul,Joshi, Mukesh C,Kumar, Vineet,Malhotra, Sanjay V.,Rawat, Diwan S.

scheme or table, p. 567 - 571 (2012/06/30)

We herein describe the synthesis of 15 novel 13-membered cyclic enediyne derivatives using simple and straightforward approach. Representative examples were screened for their anticancer activities on 60 different human tumor cell lines representing various histologies viz. leukemia, melanoma, and cancers of lung, colon, kidney, ovary, breast, prostate, and central nervous system. The enediyne derivatives with halogen substitutions, especially fluorides were found to be active against most of the cell lines. The initial results indicates marginal to good inhibition for the growth of tumor cells for several cell lines, which shows the potential of these class of compound towards anticancer application. 15 novel 13-membered cyclic enediyne derivatives using a simple and straightforward approach are synthesized. The initial results show the potential of this class of compounds towards anticancer application. Copyright

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