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HENAN SUNLAKE ENTERPRISE CORPORATIONCAS:72490-01-8 C11H15NO3//file1.lookchem.com/300w/synthetic/2022-01-30-07/844c9029-6585-4dbf-9bb6-7a410360e722.png
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CAS:72490-01-8 C11H15NO3 CAS NO.72490-01-8

Min.Order Quantity:
500 Gram
Purity:
99%
Port:
depend on clients require
Payment Terms:
L/C,T/T,

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Product Details

Keywords

  • C11H15NO3
  • CAS:72490-01-8 C11H15NO3
  • CAS:72490-01-8

Quick Details

  • ProName: CAS:72490-01-8 C11H15NO3
  • CasNo: 72490-01-8
  • Molecular Formula: C11H15NO3
  • Appearance: white poweder
  • Application: CAS:72490-01-8 C11H15NO3
  • DeliveryTime: 5 working days after cash deposit
  • PackAge: Plastic vacuum packaging bag or bucket
  • Port: depend on clients require
  • ProductionCapacity: 1 Metric Ton/Day
  • Purity: 99%
  • Storage: under the cool and dry area
  • Transportation: by express or by sea
  • LimitNum: 500 Gram
  • Grade: Industrial Grade,Pharma Grade,Electron...

Superiority

ethyl 2-(4-phenoxyphenoxy)ethylcarbamate basic information
product name: ethyl 2-(4-phenoxyphenoxy)ethylcarbamate
synonyms: ethyl 2-[p-phenoxy] ethyl carbamate;carbamic acid, 2-(4-phenoxyphenoxy)ethyl-, ethyl ester;fenoxycarb (ansi,bsi,iso);fenoxyxarb;ethyl 2-(4-phenoxyphenoxy)ethylcarbamate;fenoxycarb;ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate fenoxycarb;2-(4-phenoxyphenoxy)ethylcarbamic acid ethyl ester
cas: 72490-01-8
mf: c11h15no3
mw: 209.2417
einecs: 276-696-7
product categories: insecticide
mol file: 72490-01-8.mol
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate structure
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate chemical properties
fp 224 °c
epa substance registry system carbamic acid, [2-(4-phenoxyphenoxy)ethyl]-, ethyl ester(72490-01-8)
safety information
hazard codes n
risk statements 50/53
safety statements 60-61
rtecs fd0423000
hazardous substances data 72490-01-8(hazardous substances data)
msds information
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate usage and synthesis
usage fenoxycarb is a carbamate insect growth regulator by preventing immature insects from reaching maturity by mimicking juvenile hormone.
general description white crystalline solid. selective insecticide.
air & water reactions slightly water soluble.
reactivity profile ethyl 2-(4-phenoxyphenoxy)ethylcarbamate is a carbamate ester. carbamates are chemically similar to, but more reactive than amides. like amides they form polymers such as polyurethane resins. carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.

Details

ethyl 2-(4-phenoxyphenoxy)ethylcarbamate basic information
product name: ethyl 2-(4-phenoxyphenoxy)ethylcarbamate
synonyms: ethyl 2-[p-phenoxy] ethyl carbamate;carbamic acid, 2-(4-phenoxyphenoxy)ethyl-, ethyl ester;fenoxycarb (ansi,bsi,iso);fenoxyxarb;ethyl 2-(4-phenoxyphenoxy)ethylcarbamate;fenoxycarb;ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate fenoxycarb;2-(4-phenoxyphenoxy)ethylcarbamic acid ethyl ester
cas: 72490-01-8
mf: c11h15no3
mw: 209.2417
einecs: 276-696-7
product categories: insecticide
mol file: 72490-01-8.mol
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate structure
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate chemical properties
fp 224 °c
epa substance registry system carbamic acid, [2-(4-phenoxyphenoxy)ethyl]-, ethyl ester(72490-01-8)
safety information
hazard codes n
risk statements 50/53
safety statements 60-61
rtecs fd0423000
hazardous substances data 72490-01-8(hazardous substances data)
msds information
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate usage and synthesis
usage fenoxycarb is a carbamate insect growth regulator by preventing immature insects from reaching maturity by mimicking juvenile hormone.
general description white crystalline solid. selective insecticide.
air & water reactions slightly water soluble.
reactivity profile ethyl 2-(4-phenoxyphenoxy)ethylcarbamate is a carbamate ester. carbamates are chemically similar to, but more reactive than amides. like amides they form polymers such as polyurethane resins. carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.

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