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3766-81-2

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3766-81-2 Usage

Uses

Fenobuccarb is a carbamate insecticide used as an agricultural insecticide on rice and cotton.

Definition

Fenobucarb is a carbamate ester obtained by the formal condensation of 2-sec-butylphenol with methylcarbamic acid.

Safety Profile

Poison by ingestion, skin contact, intravenous, and intraperitoneal routes. Used as an insecticide. When heated to decomposition it emits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 3766-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3766-81:
(6*3)+(5*7)+(4*6)+(3*6)+(2*8)+(1*1)=112
112 % 10 = 2
So 3766-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-4-9(2)10-7-5-6-8-11(10)15-12(14)13-3/h5-9H,4H2,1-3H3,(H,13,14)

3766-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name fenobucarb

1.2 Other means of identification

Product number -
Other names Hopcin

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:3766-81-2 SDS

3766-81-2Synthetic route

2-sec-butylphenol
89-72-5

2-sec-butylphenol

methyl N-methylcarbamate
6642-30-4

methyl N-methylcarbamate

o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

Conditions
ConditionsYield
With trichlorophosphate at 60℃; 7-8 h;60%
formaldehyd
50-00-0

formaldehyd

o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

Chloromethyl-methyl-carbamic acid 2-sec-butyl-phenyl ester
39074-52-7

Chloromethyl-methyl-carbamic acid 2-sec-butyl-phenyl ester

Conditions
ConditionsYield
With thionyl chloride
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

2-sec-butylphenol
89-72-5

2-sec-butylphenol

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

N-Methylcarbaminsaeure-o-(1-hydroxy-1-methylpropyl)-phenylester
40137-48-2

N-Methylcarbaminsaeure-o-(1-hydroxy-1-methylpropyl)-phenylester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

Carbaminsaeure-o-sec-butylphenylester
61005-12-7

Carbaminsaeure-o-sec-butylphenylester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

N-Methylcarbaminsaeure-o-(3-hydroxy-1-methylpropyl)-phenylester
61005-16-1

N-Methylcarbaminsaeure-o-(3-hydroxy-1-methylpropyl)-phenylester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

3-(2-Methylcarbamoyloxy-phenyl)-butyric acid
61073-17-4

3-(2-Methylcarbamoyloxy-phenyl)-butyric acid

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

N-Hydroxymethylcarbaminsaeure-o-sec-butylphenylester

N-Hydroxymethylcarbaminsaeure-o-sec-butylphenylester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

Methyl-carbamic acid 2-((1S,2S)-2-hydroxy-1-methyl-propyl)-phenyl ester

Methyl-carbamic acid 2-((1S,2S)-2-hydroxy-1-methyl-propyl)-phenyl ester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

Methyl-carbamic acid 2-((1S,2R)-2-hydroxy-1-methyl-propyl)-phenyl ester

Methyl-carbamic acid 2-((1S,2R)-2-hydroxy-1-methyl-propyl)-phenyl ester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

N-Methylcarbaminsaeure-o-(1-methylacetonyl)-phenylester

N-Methylcarbaminsaeure-o-(1-methylacetonyl)-phenylester

Conditions
ConditionsYield
(microbiological transformation);
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

A

2-sec-butylphenol
89-72-5

2-sec-butylphenol

B

carbon dioxide
124-38-9

carbon dioxide

C

methylamine
74-89-5

methylamine

Conditions
ConditionsYield
With borate buffer; cetyltrimethylammonim bromide In water at 100℃; for 0.00833333h; pH=9.0; Product distribution; Further Variations:; Temperatures; Decomposition;
o-sec-butylphenyl-N-methylcarbamate
3766-81-2

o-sec-butylphenyl-N-methylcarbamate

A

2-sec-butylphenol
89-72-5

2-sec-butylphenol

B

o-hydroxyacetophenone
118-93-4

o-hydroxyacetophenone

C

2-(1-methylpropyl)phenyl formate

2-(1-methylpropyl)phenyl formate

Conditions
ConditionsYield
With dihydrogen peroxide; iron; sodium chloride In water at 25℃; Activation energy; Product distribution; Further Variations:; Temperatures; Electrolysis;

3766-81-2Relevant articles and documents

Wood preservatives

-

, (2008/06/13)

Wood preservatives having biocidal properties which include quaternary ammonium compounds of general formula (I): wherein R1 is a C8-18-alkyl group or an optionally substituted benzyl group, R2 is a C8-18-alkyl group, R3 is a C1-4-alkyl group or a group of the formula —[CH2—CH2—O]n—H, R4 is a C1-4-alkyl group, n is a number from 0.5 to 8, preferably from 1 to 5, and A?is the anion of an organic carboxylic acid which contains 2 to 12 C atoms and carries at least one hydroxyl, amino or sulfonic acid group. The wood preservatives also penetrate deeply into the wood without the use of pressure, and have only a mild corrosive action on metals. Furthermore, a process for treating timbers with these compositions, concentrates for the preparation thereof, the use of new and known quaternary ammonium compounds in wood preservatives and new quaternary ammonium compounds and their use as biocides.

Contra-thermodynamic trans-esteripication of carbamates by counter-attack strategy: A viable non-phosgene, non-mic route to carbamate pesticides

Kulkarni,Naik,Tandel,Rajappa

, p. 1249 - 1256 (2007/10/02)

Treatment of methyl N-methylcarbaaate (1, R= Me) with phosphorus oxychloride and 1-naphthol results in the formation of the transesterified product, 1-naphthyl N-methylcarbamate (2, Ar=1-naphthy 1) in good yield. Similarly, ethyl N-methylthiocarbamate (5) is converted to 1-naphthyl N-methylcarbamate (2, Ar= 1-naphthyl) on treatment with phosphorus oxychloride and 1-naphthol. The mechanism of these interesting and industrially important transformations is discussed.

Insecticidal and/or acaricidal composition exhibiting low toxicity to mammals and fish

-

, (2008/06/13)

The present invention relates to insecticidal compositions of low toxicity to fishes and mammals characterized by containing m-(p-bromophenoxy)-α-cyanobenzyl trans- or trans-rich-2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropanecarboxylate of the formula (I), STR1 and a carbamic ester of the formula (III), STR2 wherein R is a group of the formula, STR3 in which X is a C1 -C4 alkyl or C1 -C4 alkoxyl group and n is 1 or 2, in a ratio of 1 to 1-100 (part by weight) of the former to the latter, and insecticides obtained by mixing said compositions with a carrier or a diluent and if necessary an additive. The term "trans-rich" shows the ratio of trans/cis is not less than 75/25.

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