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Ethyl nitroso(prop-2-en-1-yl)carbamate, also known as ethyl N-nitrosoprop-2-enylcarbamate, is a chemical compound with the molecular formula C6H10N2O3. It is an organic nitroso compound, characterized by the presence of a nitroso group (-N=O) and a carbamate group (-O-CO-NH2). ethyl nitroso(prop-2-en-1-yl)carbamate is derived from prop-2-en-1-yl (allyl), an unsaturated three-carbon chain, and ethyl, a two-carbon alkyl group. Ethyl nitroso(prop-2-en-1-yl)carbamate is a colorless liquid with a pungent odor and is soluble in organic solvents. It is used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of pesticides and herbicides. Due to its potential reactivity and toxicity, it is important to handle ethyl nitroso(prop-2-en-1-yl)carbamate with care and in accordance with proper safety protocols.

6558-80-1

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6558-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6558-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6558-80:
(6*6)+(5*5)+(4*5)+(3*8)+(2*8)+(1*0)=121
121 % 10 = 1
So 6558-80-1 is a valid CAS Registry Number.

6558-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-nitroso-N-prop-2-enylcarbamate

1.2 Other means of identification

Product number -
Other names ethyl N-allyl-N-nirosocarbamate

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:6558-80-1 SDS

6558-80-1Upstream product

6558-80-1Downstream Products

6558-80-1Relevant academic research and scientific papers

Mild preparation of cephalosporin allyl and p-methoxybenzyl esters using diazoalkanes

Waddell, Sherman T.,Santorelli, Gina M.

, p. 1971 - 1974 (2007/10/03)

Vinyl or p-methoxyphenyldiazomethane reacts rapidly with cephalosporins in ether/methylene chloride cosolvent to give the C-9 allyl and p-methoxybenzyl esters, respectively, in good yields, with no isomerization of the double bond to Δ-2.

Organoaluminum-Promoted Homologation of Ketones with Diazoalkanes

Maruoka, Keiji,Concepcion, Arnel B.,Yamamoto, Hisashi

, p. 4725 - 4726 (2007/10/02)

Organoaluminum-promoted single homologation of aliphatic and aromatic ketones with diazoalkanes has been described, and among various organoaluminum reagents, especially bulky methylaluminum bis(2,6-di-tert-butyl-4-methylphenoxide) (MAD) is found to be highly effective for the selective homologation of various ketones.

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