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5625-96-7

5-amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile is a complex organic compound with a molecular formula of C20H20N4O4. It features a pyrazole ring, which is a five-membered aromatic ring containing four carbon atoms and one nitrogen atom. The compound has a 5-amino group, indicating the presence of an amino group at the 5th position of the pyrazole ring. Additionally, it contains a 4-carbonitrile group, which is a nitrile group (-CN) attached to the 4th position of the pyrazole ring. The compound also has a (Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl group, which is a double-bonded phenyl ring with a cyano group at the 1st position and an ethoxy-methoxy substituent at the 4th position. Lastly, it has a 1-(2-hydroxyethyl) group, which is a hydroxyethyl group attached to the 1st position of the pyrazole ring. This chemical is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a herbicide.

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  • 5-amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile

    Cas No: 5625-96-7

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  • 5625-96-7 Structure

  • Basic information

    1. Product Name: 5-amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile
    2. Synonyms: 1H-pyrazole-3-acetonitrile, 5-amino-4-cyano-alpha-[(4-ethoxy-3-methoxyphenyl)methylene]-1-(2-hydroxyethyl)-, (alphaZ)-; 5-Amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)vinyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile
    3. CAS NO:5625-96-7
    4. Molecular Formula: C18H19N5O3
    5. Molecular Weight: 353.3752
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5625-96-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 640.6°C at 760 mmHg
    3. Flash Point: 341.2°C
    4. Appearance: N/A
    5. Density: 1.26g/cm3
    6. Vapor Pressure: 2.76E-17mmHg at 25°C
    7. Refractive Index: 1.605
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile(5625-96-7)
    12. EPA Substance Registry System: 5-amino-3-[(Z)-1-cyano-2-(4-ethoxy-3-methoxyphenyl)ethenyl]-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile(5625-96-7)

  • 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: 5625-96-7(Hazardous Substances Data)

5625-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5625-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5625-96:
(6*5)+(5*6)+(4*2)+(3*5)+(2*9)+(1*6)=107
107 % 10 = 7
So 5625-96-7 is a valid CAS Registry Number.

5625-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (morpholinomethyl)hydrosilane

1.2 Other means of identification

Product number -
Other names 4-silanylmethyl-morpholine

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:5625-96-7 SDS

5625-96-7Relevant articles and documents

Reactivity of heterocyclic α-aminomethylsilanes with alcohols

Pypowski, Krzysztof,Mojzych, Mariusz

, p. 320 - 324 (2021/03/31)

[Figure not available: see fulltext.] Alkoxylation of N-substituted heterocyclic aminomethylsilyl moieties was studied using primary and tertiary alcohols. The reaction of 4-(silylmethyl)morpholine and 1-(silylmethyl)azepane under catalyst- and solvent-free conditions leads to the formation of dialkoxy- and trialkoxyaminomethylsilyl derivatives. The methanolysis of 4-(silylmethyl)morpholine resulted in trimethoxyaminomethylsilane formation as the main product and two byproducts, i.e., tetramethoxysilane and N-methylmorpholine.

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