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Home > Encyclopedia > 3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine

3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine

3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine structure

3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine 

structure
  • CAS No:

    153719-38-1

  • Formula:

    C4H8N4O3

  • Chemical Name:

    3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine

  • Synonyms:

    2H-1,3,5-Oxadiazin-4-amine,3,6-dihydro-3-methyl-N-nitro-;3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine;3-Methyl-4-nitroimino-tetrahydro-1,3,5-oxadiazine;3-Methyl-N-nitro-3,6-dihydro-2H-1,3,5-oxadiazin-4-amine

  • Categories:

    Agrochemicals  >  Pesticide Intermediates

3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine Basic Attributes

160.13

160.13

1533716-785-6

DTXSID30447146

2942000000

Characteristics

82.7

-0.6

1.6

141-143 °C

291°C

130°C

1.628

0.00201mmHg at 25°C

Safety Information

P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P321, P330, P333+P313, P363, P501

H302

|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P321, P330, P333+P313, P363, and P501|H252 (99.36%): Self-heating in large quantities; may catch fire [Warning Self-heating substances and mixtures]|P235+P410, P260, P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P314, P321, P330, P333+P313, P363, P407, P413, P420, and P501|Aggregated GHS information provided by 157 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P314, P321, P330, P333+P313, P363, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3,6-Dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine Use and Manufacturing

Methods of Manufacturing

The preparation method is that S-methyl-N-nitroisothiourea is reacted with methylamine in ethanol at 50°C, and the obtained product is reacted with formaldehyde and formic acid to obtain the product, and the reaction temperature is 90°C.

Uses

Thiamethoxam Intermediate

Computed Properties

Molecular Weight:160.13
XLogP3:-0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:160.05964013
Monoisotopic Mass:160.05964013
Topological Polar Surface Area:82.7
Heavy Atom Count:11
Complexity:186
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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