Welcome to LookChem.com Sign In|Join Free
  • or
propyl methyl(phenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77102-33-1

Post Buying Request

77102-33-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

77102-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77102-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,0 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77102-33:
(7*7)+(6*7)+(5*1)+(4*0)+(3*2)+(2*3)+(1*3)=111
111 % 10 = 1
So 77102-33-1 is a valid CAS Registry Number.

77102-33-1SDS

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 propyl N-methyl-N-phenylcarbamate

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:77102-33-1 SDS

77102-33-1Downstream Products

77102-33-1Relevant academic research and scientific papers

REACTION OF TRANSITION METAL CARBONYLS WITH HETEROCYCLIC SYSTEMS. VI. THE INTERACTION OF Fe2(CO)9 WITH N-BENZYLOXYPIPERIDINE AND RELATED COMPOUNDS

Blum, Y.,Becker, Y.,Shvo, Y.

, p. 65 - 76 (2007/10/02)

N-Benzyloxypiperidine exhibits an unexpected type of reactivity toward Fe2(CO)9.Benzaldehyde and N-formylpiperidine are formed, most probably in a concerted manner, as revealed by deuterium-labeling experiments.Several mechanistic details of this reaction have been elucidated.The nature of the reaction contrasts with that of N-propyloxy-N-methylaniline, which upon treatment with Fe2(CO)9 undergoes insertion of a CO group into the N-O bond to generate a carbamate.

A chemical confirmatory test for organophosphorus and carbamate insecticides and triazine and urea herbicides with reactive NH moieties

Greenhalgh,Kovacicova

, p. 325 - 330 (2007/10/09)

The effects of different solvents and temperatures on the base catalyzed reaction of O,O-diethyl N-methyl phosphoramidothioate and methyl iodide were studied. The N-methyl derivative was obtained in high yield in dimethyl sulfoxide at 50° for 10 min with sodium hydride as the base. This alkylation procedure was adapted to the microgram level and applied to 16 insecticides and herbicides which have an NH or NH2 moiety. With carbamates, the best yields were obtained when the reaction was carried out at room temperature. The alkylated derivatives of organophosphorus and carbamate insecticides and triazine and urea herbicides all had better gc characteristics than the parent compounds. Thus, the alkylureas readily chromatographed on SE-30/QF-1 under conditions where the parent compounds decomposed. On this column, the alkylated phosphoramidothioates and carbamates also had shorter retention times. Alkylation of crude extracts of soil, plants, and blood plasma containing herbicides and insecticides illustrated the ability of the sodium hydride methyl iodide dimethyl sulfoxide procedure to confirm the identity of residues at the sub parts per million level.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 77102-33-1