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71516-49-9

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71516-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71516-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,1 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71516-49:
(7*7)+(6*1)+(5*5)+(4*1)+(3*6)+(2*4)+(1*9)=119
119 % 10 = 9
So 71516-49-9 is a valid CAS Registry Number.

71516-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-benzyloxyethyl)-1,3-dioxolane

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:71516-49-9 SDS

71516-49-9Relevant articles and documents

Aminopolycarboxylic acids and derivatives thereof

-

, (2008/06/13)

There are provided chelating agents particularly useful for the preparation of diagnostic and therapeutic agents for magnetic resonance imaging, scintigraphy, ultrasound imaging, radiotherapy and heavy metal detoxification, said agents being compounds of formula I wherein n and m are 2, 3 or 4; and A, X, R1 and Z are as defined in the specification.

Synthesis and Use of 7-Substituted Norbornadienes for the Preparation of Prostaglandins and Prostanoids

Baxter, Anthony D.,Binns, Falmai,Javed, Tariq,Roberts, Stanley M.,Sadler, Peter,et al.

, p. 889 - 900 (2007/10/02)

Syntheses of 7-substituted norbornadienes from 7-t-butoxy- and 7-halogeno-norbornadienes are described.Rearrangement of the products in the presence of peracetic acid gives bicyclic aldehydes (2) in equilibrium with enol ethers (3) which are hydrolysed to hydroxycyclopentenylacetaldehydes (4), and converted into key intermediates for the synthesis of prostaglandins and their analogues.Syntheses of prostaglandin J analogues with n-hexyl and phenyl groups replacing the ο-side-chain are described.

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