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Trimethylsilyl dihydrogen phosphate, also known as (trimethylsilyl)phosphonic acid or trimethylsilyl hydrogen phosphate, is a chemical compound with the formula (CH3)3SiH2PO4. It is a colorless, hygroscopic liquid that is soluble in organic solvents. Trimethylsilyl dihydrogen phosphate is an important reagent in organic synthesis, particularly for the protection of phosphate groups in biological molecules. It is also used as a coupling agent in the formation of organophosphorus compounds and as a silylating agent in various chemical reactions. Trimethylsilyl dihydrogen phosphate is synthesized by the reaction of trimethylsilyl chloride with phosphoric acid or its derivatives. Due to its reactivity and potential hazards, it is essential to handle Trimethylsilyl dihydrogen phosphate with care, following proper safety protocols.

7422-66-4

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7422-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7422-66-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7422-66:
(6*7)+(5*4)+(4*2)+(3*2)+(2*6)+(1*6)=94
94 % 10 = 4
So 7422-66-4 is a valid CAS Registry Number.

7422-66-4SDS

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 trimethylsilyl dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names phosphoric acid mono-trimethylsilanyl ester

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:7422-66-4 SDS

7422-66-4Relevant academic research and scientific papers

Benzoxa condensed ring compounds, process for producing the same and pharmaceutical composition comprising the same

-

, (2008/06/13)

Pharmaceutical compositions containing a benzoxazole compound and a 2,3-dihydrobenzofuran compound represented by the following formula (I) and its pharmaceutically acceptable salt: STR1 In the formula, any one of P, Q, R and S is a group represented by t

Para ordered aromatic diacids containing benzimidazole groups

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, (2008/06/13)

2-Benzimidazole terephthalic acid, 4,4'-dicarboxy-2,2'-bisbenzimidazole benyl and 4,4"-dicarboxy-2'-phenyl-3'-[2-(4-phenylbenzthiazole)]-6'-[2-(3-phenylbenzimidazole]-p-terphenyl are provided. Also provided are methods for preparing these dicarboxylic acids. 2-benzimidazole terephthalic acid is prepared by reacting trimellitic anhydride with o-phenylenediamine in a suitable solvent. 4,4'-dicarboxy-2,2'-bisbenzimidazole biphenyl is prepared by diazotizing 2-amino-5-bromobenzoic acid to prepare 4,4'-dibromodiphenic acid, reacting the 4,4'-dibromodiphenic acid with o-phenylenediamine in trimethylsilyl polyphosphate solution to prepare 4,4'-dibromo-2,2'-bisbenzimidazolyl biphenyl, reacting the 4,4'-dibromo-2,2'-bisbenzimidazolyl biphenyl with cuprous cyanide to prepare the corresponding dicyano compound, and hydrolyzing the dicyano compound. 4,4"-Dicarboxy-2'-phenyl-3'-[2-(4-phenylbenzthiazole)]-6'-[2-(3-phenylbenzimidazole)]-p-terphenyl is prepared by reacting a 4-benzazole benzil with 1,3-bis(p-bromophenyl)-2-propanone to prepare 2,5-bis(p-bromophenyl)-3-phenyl-4-(2-phenylbenzazole) cyclopentadienone, reacting the cyclopentadienone with 2-(3-ethynylphenyl) benzimidazole to prepare the corresponding dibromo terphenyl compound, reacting the dibromo terphenyl compound with cuprous cyanide to prepare the corresponding dicyano terphenyl compound, and hydrolyzing the dicyano compound.

Benzoxazole derivatives

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, (2008/06/13)

Novel benzoxazole derivative of the formula: STR1 wherein R is a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted cycloalkyl group or a substituted or unsubstituted heterocyclic group; Alk is single bond, a substituted or unsubstituted lower alkylene group, a lower alkenylene group or a lower alkynylene group; the group STR2 is a group of the formula: --CH2 -- or --CH=, and a pharmaceutically aceptable salt thereof are disclosed. Said derivative (I) and a salt thereof are useful as therapeutic agents for diabetes.

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