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Ethyl 3-dimethylamino-2-formylacrylate, with the CAS number 61749-94-0, is a specialized organic compound characterized by its formula C9H15NO3 and a molecular weight of 185.22. It is a complex chemical entity with multiple functional groups, including the dimethylamino group and the formylacrylate group. Although not widely studied or used in commercial products, this compound is primarily utilized in scientific research.

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  • 92385-43-8 Structure
  • Basic information

    1. Product Name: Ethyl 3-dimethylamino-2-formylacrylate
    2. Synonyms: Ethyl 3-N,N-dimethylamino-2-formylacrylate;ETHYL 3-DIMETHYLAMINO-2-FORMYLACRYLATE;3-(Dimethylamino)-2-formyl-2-propenoic acid ethyl ester;BWSIQAALZBOBQJ-UHFFFAOYSA-N
    3. CAS NO:92385-43-8
    4. Molecular Formula: C8H13NO3
    5. Molecular Weight: 171.19
    6. EINECS: N/A
    7. Product Categories: Aliphatic Compound
    8. Mol File: 92385-43-8.mol
  • Chemical Properties

    1. Melting Point: 149-150 °C
    2. Boiling Point: 366.913 °C at 760 mmHg
    3. Flash Point: 175.703 °C
    4. Appearance: /
    5. Density: 1.056
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.464
    8. Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: Ethyl 3-dimethylamino-2-formylacrylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Ethyl 3-dimethylamino-2-formylacrylate(92385-43-8)
    12. EPA Substance Registry System: Ethyl 3-dimethylamino-2-formylacrylate(92385-43-8)
  • 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: 92385-43-8(Hazardous Substances Data)

92385-43-8 Usage

Uses

Used in Scientific Research:
Ethyl 3-dimethylamino-2-formylacrylate is used as a research chemical for [application reason], contributing to the advancement of organic chemistry and the exploration of its potential applications in various fields. Due to its complex structure and multiple functional groups, it serves as a valuable compound for studying chemical reactions and interactions. The stability, reactivity, and potential health hazards of Ethyl 3-dimethylamino-2-formylacrylate are yet to be thoroughly investigated, making it an intriguing subject for scientific inquiry.

Check Digit Verification of cas no

The CAS Registry Mumber 92385-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,8 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92385-43:
(7*9)+(6*2)+(5*3)+(4*8)+(3*5)+(2*4)+(1*3)=148
148 % 10 = 8
So 92385-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO3/c1-4-12-8(11)7(6-10)5-9(2)3/h5-6H,4H2,1-3H3/b7-5+

92385-43-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-(dimethylamino)-2-formylacrylate

1.2 Other means of identification

Product number -
Other names ethyl 3-(dimethylamino)-2-formylprop-2-enoate

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:92385-43-8 SDS

92385-43-8Relevant articles and documents

A novel series of potent and selective small molecule inhibitors of the complement component C1s

Subasinghe, Nalin L.,Ali, Farah,Illig, Carl R.,Rudolph, M. Jonathan,Klein, Scott,Khalil, Ehab,Soll, Richard M.,Bone, Roger F.,Spurlino, John C.,DesJarlais, Renee L.,Crysler, Carl S.,Cummings, Maxwell D.,Morris Jr., Philip E.,Kilpatrick, John M.,Babu, Y. Sudhakara

, p. 3043 - 3047 (2007/10/03)

Activation of the classical pathway of complement has been implicated in disease states such as hereditary angioedema, ischemia-reperfusion injury and acute transplant rejection. The trypsin-like serine protease C1s represents a pivotal upstream point of

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