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2536-36-9

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2536-36-9 Usage

Chemical Properties

Colourless solid

Check Digit Verification of cas no

The CAS Registry Mumber 2536-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2536-36:
(6*2)+(5*5)+(4*3)+(3*6)+(2*3)+(1*6)=79
79 % 10 = 9
So 2536-36-9 is a valid CAS Registry Number.

2536-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name IHDA

1.2 Other means of identification

Product number -
Other names 16-Jod-hexadecansaeure

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:2536-36-9 SDS

2536-36-9Relevant articles and documents

CT CONTRAST AGENT FOR DETECTION OF CACHEXIA

-

Page/Page column 43-44, (2020/08/28)

The invention relates to an iodinated CT contrast agent for non-invasive diagnosis of cachexia. This is possible by superior resolution of CT combined with CT contrast agent specific for the brown and/or beige adipose tissue (BAT).

Regio- and chemoselective one-step 3-O-alkylenation of unprotected ascorbic acid using ω-iodoalkanols

Muller, Thierry,Heuschling, Paul,Luu, Bang

experimental part, p. 217 - 220 (2009/06/05)

A regio- and chemoselective alkylenation employing unprotected ascorbic acid and a series of unprotected iodoalkanols in the presence of sodium hydrogen carbonate in dimethyl sulfoxide is described. This atom economic high yielding procedure delivers the

Design and synthesis of asymmetric acyclic phospholipid bolaamphiphiles

Kai, Toshitsugu,Sun, Xue-Long,Faucher, Keith M.,Apkarian, Robert P.,Chaikof, Elliot L.

, p. 2606 - 2615 (2007/10/03)

(Chemical Equation Presented) A synthetic route was devised for the generation of asymmetric lipid bolaamphiphiles through the sequential esterification of an alkyldioic acid, bearing distinct terminal protecting groups, with propanylamine and lyso-phosph

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