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500878-72-8

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500878-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500878-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,8,7 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 500878-72:
(8*5)+(7*0)+(6*0)+(5*8)+(4*7)+(3*8)+(2*7)+(1*2)=148
148 % 10 = 8
So 500878-72-8 is a valid CAS Registry Number.

500878-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-((4-methoxyphenyl)diphenylmethoxy)pentan-1-ol

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:500878-72-8 SDS

500878-72-8Relevant articles and documents

Facilitated photochemical cleavage of benzylic C-O bond. Application to photolabile hydroxyl-protecting group design

Wang, Pengfei,Zhou, Lei,Zhang, Xin,Liang, Xing

scheme or table, p. 1514 - 1516 (2010/06/12)

A new photolabile hydroxyl-protecting group has been developed by introducing a dimethylamino group to the meta position of an aromatic ring of the traditional trityl (Tr) protecting group. The Royal Society of Chemistry 2010.

Synthesis of spirobicyclic peptides on a solid support

Virta, Pasi,Sinkkonen, Jari,Loennberg, Harri

, p. 3616 - 3621 (2007/10/03)

The spirobicyclic peptides 2-6 were synthesized as stereoisomeric pairs using an orthogonally protected bis(aminomethyl)malonic acid building block 1 as the branching unit. Peptide 2 was synthesized by two methods. Either the chain assembly and first cyclization were carried out on a Wang resin, and the second cyclization in solution (Scheme 1), or the whole synthesis was performed on a solid-supported backbone amide linker derived from 4-alkoxybenzaldehyde (Scheme 3). The applicability of the latter method was further evaluated by synthesis of four additional spirobicyclic peptides 3-6.

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