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Benzenamine, N-(2-propenyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

558484-57-4

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558484-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 558484-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,8,4,8 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 558484-57:
(8*5)+(7*5)+(6*8)+(5*4)+(4*8)+(3*4)+(2*5)+(1*7)=204
204 % 10 = 4
So 558484-57-4 is a valid CAS Registry Number.

558484-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name O-allyl-N-phenylhydroxylamine

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:558484-57-4 SDS

558484-57-4Downstream Products

558484-57-4Relevant academic research and scientific papers

Allylboration of nitrosobenzene

Bubnov, Yurii N.,Pershin, Dmitrii G.,Karionova, Anna L.,Gurskii, Mikhail E.

, p. 202 - 203 (2007/10/03)

The allylboration of nitrosobenzene at -70°C resulted in the formation of N- and O-allyl derivatives of N-phenylhydrazine, which were reduced with the second allylborane molecule to N-allylaniline above 100°C.

Reductive reactions of nitroarenes in the presence of allyl bromide and zinc dust

Kim, Byeong Hyo,Kim, Tae Kyu,Cheong, Jae Wook,Lee, Sang Woo,Jun, Young Moo,Baik, Woonphil,Lee, Byung Min

, p. 1921 - 1928 (2007/10/03)

Under the mild condition, allyl bromide/Zn mediated reductive N,O- diallylation of nitrobenzene was observed. In case of o-nitroarenes such as 2-nitrobenzaldehyde derivatives, 2'-nitroacetophenone, and N-(2- nitrobenzylidene)anilines, reductive cyclizations were accomplished in good to excellent yields. Synthesis and mechanistic details are discussed.

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