trans-4-Methoxycinnamoyl chloride - ≥97% , CAS No.42996-84-9

CAS: 42996-84-9 Cat. No.: T344906 Molecular Weight: 196.64 EC Number: 626-984-7 PubChem CID: 10976422
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
p-Methoxycinnamic acid chloride | MFCD00039314 | AKOS005173513 | 4-methoxycinnamoylchloride | trans-3-(4-Methoxyphenyl)-acryloyl chloride | (E)-4-methoxycinnamoyl chloride | trans-3-(4-Methoxyphenyl)-acryloyl chloride | (E)-3-(4-Methoxyphenyl)acryloyl ch
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
T344906-1g
1

$108.90

$163.90
Save $55.00 (33.56%)
5g
T344906-5g
1

$379.90

$569.90
Save $190.00 (33.34%)
25g
T344906-25g
1

$1,232.90

$1,849.90
Save $617.00 (33.35%)
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Trans-4-methoxycinnamoyl chloride is a widely used compound. Its main role is to be used as a reagent in organic synthesis to promote the production of a variety of compounds. It is practical in polymer synthesis and preparation of various materials. As an acyl chloride, trans-4-methoxycinnamoyl chloride has the characteristics of an acylating agent. This allows it to react with primary and secondary amines to form amides. In addition, it can also react with alcohols to form esters, and react with thiols to form thioesters. These chemical reactions can synthesize a variety of compounds and contribute to the versatility of trans-4-methoxycinnamoyl chloride in scientific research.

Specifications

Synonyms
p-Methoxycinnamic acid chloride | MFCD00039314 | AKOS005173513 | 4-methoxycinnamoylchloride | trans-3-(4-Methoxyphenyl)-acryloyl chloride | (E)-4-methoxycinnamoyl chloride | trans-3-(4-Methoxyphenyl)-acryloyl chloride | (E)-3-(4-Methoxyphenyl)acryloyl ch
Specifications & Purity
≥97%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%
Names and Identifiers
Canonical SmilesCOC1=CC=C(C=C1)C=CC(=O)Cl
IUPAC Name(E)-3-(4-methoxyphenyl)prop-2-enoyl chloride
InChIKeyCGOJOQBYEAVATL-QPJJXVBHSA-N
INCHI1S/C10H9ClO2/c1-13-9-5-2-8(3-6-9)4-7-10(11)12/h2-7H,1H3/b7-4+
Isomeric SMILES COC1=CC=C(C=C1)/C=C/C(=O)Cl
PubChem CID 10976422
UN Number 3261
Packing Group II
Molecular Weight 196.64

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClassCinnamic acids and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentCinnamic acids and derivatives
Alternative Parents Styrenes  Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  Acyl chlorides  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Cinnamic acid or derivatives - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Styrene - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Ether - Acyl chloride - Acyl halide - Organochloride - Organohalogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeDateItem
B2520549Certificate of AnalysisFeb 07, 2025 T344906
B2520556Certificate of AnalysisFeb 07, 2025 T344906
B2520557Certificate of AnalysisFeb 07, 2025 T344906
B2520558Certificate of AnalysisFeb 07, 2025 T344906
B2520559Certificate of AnalysisFeb 07, 2025 T344906
B2520563Certificate of AnalysisFeb 07, 2025 T344906
Chemical and Physical Properties
Molecular Weight196.630 g/mol
XLogP32.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass196.029 Da
Monoisotopic Mass196.029 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count13
Formal Charge0
Complexity193.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Solution Calculators
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