118653-15-9

• 

• Basic information

  1. Product Name: 2-Propenamide, 3-(2-methoxyphenyl)-, (Z)-
  2. Synonyms:
  3. CAS NO:118653-15-9
  4. Molecular Formula: C10H11NO2
  5. Molecular Weight: 177.203
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 118653-15-9.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 2-Propenamide, 3-(2-methoxyphenyl)-, (Z)-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-Propenamide, 3-(2-methoxyphenyl)-, (Z)-(118653-15-9)
  11. EPA Substance Registry System: 2-Propenamide, 3-(2-methoxyphenyl)-, (Z)-(118653-15-9)

• 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: 118653-15-9(Hazardous Substances Data)

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• 2-Propenamide, 3-(2-methoxyphenyl)-, (Z)-

  Cas No: 118653-15-9

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  Cas No: 118653-15-9

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118653-15-9 Usage

General Description

2-Propenamide, 3-(2-methoxyphenyl)-, (Z)- is a chemical compound with the molecular formula C10H11NO2. It is also known as (Z)-3-(2-methoxyphenyl)acrylamide and is characterized by a Z isomerism. 2-Propenamide, 3-(2-methoxyphenyl)-, (Z)- is a colorless to pale yellow liquid with a strong odor. It is often used in various industrial and pharmaceutical applications, including as a raw material for the synthesis of other organic compounds. Additionally, it may have potential uses in the field of organic chemistry and medicinal research due to its unique chemical structure and properties. However, it is important to handle and use this chemical with care, as it may have certain health and environmental risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 118653-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,5 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118653-15:
(8*1)+(7*1)+(6*8)+(5*6)+(4*5)+(3*3)+(2*1)+(1*5)=129
129 % 10 = 9
So 118653-15-9 is a valid CAS Registry Number.

118653-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-(2-methoxyphenyl)prop-2-enamide

1.2 Other means of identification

Product number	-
Other names	2-Methoxy-cis-zimtsaeure-amid

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:118653-15-9 SDS

118653-15-9Upstream product

• 118678-22-1 C₁₃H₁₄O₅ 
• 144393-52-2 (E)-3-(2-methoxyphenyl)acrylamide 
• 683-57-8 bromo-acetic acid amide 
• 135-02-4 ortho-anisaldehyde 
• 14737-91-8 (Z)-o-methoxycinnamic acid 

118653-15-9Downstream Products

118653-15-9Relevant articles and documents

Photocatalyst-free visible light promoted: E → Z isomerization of alkenes

Xu, Jianbin,Liu, Na,Lv, Haiping,He, Chixian,Liu, Zining,Shen, Xianfu,Cheng, Feixiang,Fan, Baomin

, p. 2739 - 2743 (2020)

A simple and green method of visible light driven photocatalytic E to Z isomerization of alkenes has been developed. A variety of (Z)-alkenes can be prepared in the presence of visible light, without any additional photocatalyst. This protocol features photocatalyst-free conditions, which are mild, tolerant, and operationally simple, and is easy to implement.

Synthesis of Enamides

Brettle, Roger,Mosedale, Alan J.

, p. 2185 - 2196 (2007/10/02)

(Z)-3-Arylprop-2-enoic acids can be converted by the Curtius procedure, through the acyl azides, into (Z)-2-arylethenyl isocyanates, which with methanol give methyl (Z)-N-(2-arylethenyl)carbamates.Acylation of the (Z)-enecarbamates, through their anions, leads to methyl (Z)-N-acyl-N-(2-arylethenyl)carbamates, which on treatment with lithium iodide in boiling N,N-dimethylformamide or acetonitrile undergo demethoxycarbonylation to give (Z)-enamides.The stereospecific route to enamides can also be used in the E-series.Treatment of (Z)- or (E)-2-arylethenyl isocyanates with trifluoroacetic acid gives (E)-N-(2-arylethenyl)trifluoroacetamides,the anions of which, with acylating agents, give (E)-enamides directly.

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