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4-BENZYLOXYPHENYLISOCYANIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

356533-74-9

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356533-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356533-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,5,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 356533-74:
(8*3)+(7*5)+(6*6)+(5*5)+(4*3)+(3*3)+(2*7)+(1*4)=159
159 % 10 = 9
So 356533-74-9 is a valid CAS Registry Number.

356533-74-9SDS

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 4-BENZYLOXYPHENYLISOCYANIDE

1.2 Other means of identification

Product number -
Other names HANSA ISN-0054

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:356533-74-9 SDS

356533-74-9Downstream Products

356533-74-9Relevant academic research and scientific papers

Rational design and synthesis of 1,5-disubstituted tetrazoles as potent inhibitors of the MDM2-p53 interaction

Surmiak, Ewa,Neochoritis, Constantinos G.,Musielak, Bogdan,Twarda-Clapa, Aleksandra,Kurpiewska, Katarzyna,Dubin, Grzegorz,Camacho, Carlos,Holak, Tad A.,D?mling, Alexander

, p. 384 - 407 (2016/12/22)

Using the computational pharmacophore-based ANCHOR.QUERY platform a new scaffold was discovered. Potent compounds evolved inhibiting the protein-protein interaction p53-MDM2. An extensive SAR study was performed based on our four-point pharmacophore model

Synthesis of isonitriles from N-substituted formamides using triphenylphosphine and iodine

Wang, Xia,Wang, Qing-Gang,Luo, Qun-Li

, p. 49 - 54 (2015/02/02)

Treatment of N-substituted formamides with the reagent combination of triphenylphosphine and molecular iodine, in the presence of a tertiary amine, quickly produces the corresponding isocyanides in high yields under ambient conditions. The process employs readily available and low-cost reagents, a convenient synthetic procedure, and mild reaction conditions for the synthesis of various alkyl and aryl isocyanides.

A novel method for preparing isocyanides from N-substituted formamides with chlorophosphate compounds

Kobayashi, Genki,Saito, Tateo,Kitano, Yoshikazu

, p. 3225 - 3234 (2011/11/30)

Treatment of N-substituted formamides with chlorophosphate compounds such as PhOPOCl2, EtOPOCl2, Me2NPOCl2, and (PhO)2POCl and tertiary amines such as triethylamine, pyridine, and N,N-diisopropylethylamine produced the corresponding isocyanides in high yields. This method can be used to prepare various alkyl and aryl isocyanides. Georg Thieme Verlag Stuttgart · New York.

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