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352530-52-0

((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE, also known as o-Methylamino-2-nitrovinylmethane, is a chemical compound with the molecular formula C4H8N2O3. It is a yellow liquid with the chemical structure CH3OCH=CHNO2CH2NH2.
Used in Pharmaceutical Industry:
((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various medicinal compounds.
Used in Agricultural Chemicals Industry:
((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE is used as an intermediate in the synthesis of agricultural chemicals to aid in the production of effective crop protection agents.
Used in Organic Synthesis:
((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE is used as a building block in organic synthesis, enabling the creation of a range of organic compounds for various applications.
Used in Fine Chemicals Production:
((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE is used in the production of fine chemicals, where its reactive properties are harnessed to produce high-quality specialty chemicals.

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  • 352530-52-0 Structure

  • Basic information

    1. Product Name: ((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE
    2. Synonyms: (E)-1-methoxy-N-methyl-2-nitroethenamine
    3. CAS NO:352530-52-0
    4. Molecular Formula: O2NCH=C(OCH3)NHCH3
    5. Molecular Weight: 132.12
    6. EINECS: N/A
    7. Product Categories: Enol Ethers;Organic Building Blocks;Oxygen Compounds;Building Blocks;Chemical Synthesis;Enol Ethers;Organic Building Blocks;Oxygen Compounds
    8. Mol File: 352530-52-0.mol

  • Chemical Properties

    1. Melting Point: 116-120 °C(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: ((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE(352530-52-0)
    11. EPA Substance Registry System: ((1E)-1-METHOXY-2-NITROVINYL)METHYLAMINE(352530-52-0)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 352530-52-0(Hazardous Substances Data)

352530-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352530-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 352530-52:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*0)+(2*5)+(1*2)=120
120 % 10 = 0
So 352530-52-0 is a valid CAS Registry Number.

352530-52-0 Well-known Company Product Price

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  • Aldrich

  • (540420)  [(1E)-1-Methoxy-2-nitrovinyl]methylamine  95%

  • 352530-52-0

  • 540420-25G

  • 1,879.02CNY

  • Detail

352530-52-0SDS

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 2-methoxy-3-nitroprop-2-en-1-amine

1.2 Other means of identification

Product number -
Other names -

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:352530-52-0 SDS

352530-52-0Downstream Products

352530-52-0Relevant articles and documents

An anomalous hydration/dehydration sequence for the mild generation of a nitrile oxide

Nishiwaki, Nagatoshi,Kobiro, Kazuya,Kiyoto, Hideyuki,Hirao, Shotaro,Sawayama, Jun,Saigo, Kazuhiko,Okajima, Yoshikazu,Uehara, Toshiharu,Maki, Asaka,Ariga, Masahiro

experimental part, p. 2832 - 2839 (2011/05/04)

A nitrile oxide containing a carbamoyl group is readily generated upon the treatment of 2-methyl-4-nitro-3-isoxazolin-5(2H)-one with water under mild reaction conditions, even in the absence of special reagents. The obtained nitrile oxide undergoes cycloa

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