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6-chloro-2,4-diethoxy-pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93232-55-4

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93232-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93232-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93232-55:
(7*9)+(6*3)+(5*2)+(4*3)+(3*2)+(2*5)+(1*5)=124
124 % 10 = 4
So 93232-55-4 is a valid CAS Registry Number.

93232-55-4SDS

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 4-chloro-2,6-diethoxypyrimidine

1.2 Other means of identification

Product number -
Other names Pyrimidine,4-chloro-2,6-diethoxy

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:93232-55-4 SDS

93232-55-4Downstream Products

93232-55-4Relevant academic research and scientific papers

De novo design of nonpeptidic compounds targeting the interactions between interferon-α and its cognate cell surface receptor

Bello, Angelica M.,Bende, Tanushree,Wei, Lianhu,Wang, Xiaoyang,Majchrzak-Kita, Beata,Fish, Eleanor N.,Kotra, Lakshmi P.

, p. 2734 - 2743 (2008/12/22)

Type 1 interferons (IFN) bind specifically to the corresponding receptor, IFNAR. Agonists and antagonists for IFNAR have potential therapeutic value in the treatment of viral infections and systemic lupus erythematosus, respectively. Specific sequences on

Fluorine-free titanocenes and the use thereof

-

, (2008/06/13)

Fluorine-free titanocene compounds of the formula I or II STR1 in which both R1 radicals are preferably, independently of one another, cyclopentadienyl?, which is unsubstituted or substituted by alkyl,alkoxy or --Si(R2)3, and both R2 radicals are, in particular, alkyl, STR2 Z is --NR10 --, --0-- or --S--, Y is Cl, Br, I, CN, SCN, --O--CO--CH3, --O--CO--phenyl or --O--SO2 --CH3, n is 1 or 2, m is 0 or 1, where the sum of n and m must be 2, R3, R4 and R5 are in particular, independently of one another, hydrogen, Cl, alkyl, cycloalkyl, adamantyl, phenyl, pyrryl or biphenylyl, where these radicals are unsubstituted or substituted by alkyl, Cl, alkylthio, --NR8 R9, phenyl, phenylthio or C1 -C10 alkoxy, or R3, R4 and R5 are alkenyl, alkoxy, cycloalkoxy, phenoxy, benzyloxy, tetrahydrofurfuryloxy, alkylthio, cycloalkylthio, benzylthio or phenylthio, where R3 and R4 are not simultaneously hydrogen, and if Q is a pyrimidyl radical, at least one radical R3 or R4 is alkoxy, cycloalkoxy, phenoxy, benzyloxy, tetrahydrofurfuryloxy or alkenyloxy, and if Z is --NR10 --, R3 and R4 are Cl Br or I, both radicals R6, independently of one another, are alkyl or alkenyl or both radicals R6 together with the nitrogen atom to which they are bonded, form a morpholino radical, R7 is alkyl, cycloalkyl or phenyl, R8 is phenyl or α-tertiary C4 -C6 alkyl, R9 is, in particular, hydrogen, alkyl, cycloalkyl, phenyl or a STR3 radical, where, in addition, the two R9 radicals in --N(R9)2 are identical or different and, together with the nitrogen atom to which they are bonded, may form a 5- or 6-membered heterocyclic ring which, in addition to the nitrogen atom, may also contain further nitrogen, oxygen or sulfur atoms, R10 is as defined for R9 or additionally, in particular, is phenyl which is unsubstituted or substituted by Cl, C1 -C12 alkyl, C1 -C10 alkoxy, C1 -C8 alkylthio, phenylthio, morpholino or --N(C1 -C4 alkyl)2, X is --O--, --S--, STR4 methylene or ethylene, and A is C1 -C12 alkylene or --X--A--X-- is a direct bond, are suitable as photoinitiators for photopolymerisation of compounds containing ethylenically unsaturated double bonds.

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