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10570-48-6

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10570-48-6 Usage

General Description

DIMETHYL(4-METHOXYPHENYLOXOMETHYL)PHOSPHONATE is a chemical compound containing a phosphonate group and a methoxy-substituted benzyl group. It is an organophosphorus compound commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. DIMETHYL(4-METHOXYPHENYLOXOMETHYL)PHOSPHONATE is often used as a reagent in organic synthesis due to its ability to act as a phosphonate protecting group in various reactions. It is important to handle this chemical with caution, as it can be harmful if ingested, inhaled, or comes into contact with skin, and proper safety precautions should be taken when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 10570-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10570-48:
(7*1)+(6*0)+(5*5)+(4*7)+(3*0)+(2*4)+(1*8)=76
76 % 10 = 6
So 10570-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H13O5P/c1-13-9-6-4-8(5-7-9)10(11)16(12,14-2)15-3/h4-7H,1-3H3

10570-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethoxyphosphoryl-(4-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names <4-Methoxy-benzoyl>-phosphonsaeure-dimethylester

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:10570-48-6 SDS

10570-48-6Relevant articles and documents

Kluger,Chin

, p. 7382,7383-7385 (1978)

Phosphorus compounds as photoinitiators for radicalic polymerization

Macarie, Lavinia,Ilia,Iliescu, Smaranda,Popa, Adriana,Dehelean,Manoviciu,Petrean,Abadie

, p. 165/[421]-173/[429] (2004)

p-Methoxybenzoyldialkylphosphonates, where alkyl = methyl, ethyl and p-methoxy-benzoyldiphenylphosphine oxide were synthesized by Michaelis-Arbuzov reaction. These compounds were used as photoinitiators for radicalic polymerization of acrylic monomers. Th

Selective P?C(sp3) Bond Cleavage and Radical Alkynylation of α-Phosphorus Alcohols by Photoredox Catalysis

Jia, Kunfang,Li, Junzhao,Chen, Yiyun

supporting information, p. 3174 - 3177 (2018/02/09)

Herein the first P?C(sp3) bond cleavage and radical alkynylation of α-phosphorus alcohols to construct phosphonoalkynes is reported. The phosphorus radical is generated upon P?C bond cleavage reaction via the alkoxyl radical through photoredox catalysis with cyclic iodine(III) reagents. Various arylphosphinoyl-, alkylphosphinoyl-, phosphonate-, and phosphonic amide alcohols serve as radical phosphorus precursors to construct phosphonoalkynes for the first time.

Reactions of acyl phosphonates with organoaluminum reagents: A new method for the synthesis of secondary and tertiary α-hydroxy phosphonates

Seven, Ozlem,Polat-Cakir, Sidika,Hossain, Md. Shakhawoat,Emrullahoglu, Mustafa,Demir, Ayhan S.

body text, p. 3464 - 3469 (2011/06/19)

The reactions of organoaluminum reagents (trimethylaluminum, triethylaluminum, etc.) with aryl and alkyl acyl phosphonates, which lead to the formation of α-hydroxy phosphonates in moderate to good yields, are reported. This method provides easy access to

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