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75499-99-9

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75499-99-9 Usage

General Description

2,4(1H,3H)-Pyrimidinedione, 1,3-bis[(phenylmethoxy)methyl]- is a chemical compound with a pyrimidine ring structure. It contains two bis[(phenylmethoxy)methyl] groups, which are linked to the 1 and 3 positions of the pyrimidine ring. 2,4(1H,3H)-Pyrimidinedione, 1,3-bis[(phenylmethoxy)methyl]- is often used as a reagent in organic synthesis and pharmaceutical research. Its properties make it suitable for a variety of applications, including as a building block for the synthesis of new compounds with potential biological activity. Additionally, its structure suggests potential applications in the development of pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 75499-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,9 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75499-99:
(7*7)+(6*5)+(5*4)+(4*9)+(3*9)+(2*9)+(1*9)=189
189 % 10 = 9
So 75499-99-9 is a valid CAS Registry Number.

75499-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H,1H,2H,2H-pentadecafluoro-nonan-1-ol

1.2 Other means of identification

Product number -
Other names Telomer alcohol-L

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:75499-99-9 SDS

75499-99-9Relevant articles and documents

Synthesis of chiral carbocyclic ribonucleotides

Antle, Vincent D.,Caperelli, Carol A.

, p. 1911 - 1928 (2007/10/03)

The carbocyclic analogs of CMP, UMP, GMP, IMP, and ribo-TMP, of the same absolute configuration as the naturally occurring β-D-ribofuranose-based ribonucleoside monophosphates, have been synthesized. The synthetic route employed Mitsunobu coupling of the

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