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2622-08-4

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2622-08-4 Usage

Uses

Tri(o-tolyl) phosphite is?used as a plasticizer and in?organic synthesis.

Safety Profile

Poison by subcutaneous route.When heated to decomposition it emits toxic fumes ofPOx.

Check Digit Verification of cas no

The CAS Registry Mumber 2622-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2622-08:
(6*2)+(5*6)+(4*2)+(3*2)+(2*0)+(1*8)=64
64 % 10 = 4
So 2622-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H21O6P/c22-19-10-4-1-7-16(19)13-25-28(26-14-17-8-2-5-11-20(17)23)27-15-18-9-3-6-12-21(18)24/h1-12,22-24H,13-15H2

2622-08-4 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (10258)  Tri(o-tolyl) phosphite, typically C 71%, H 6%   

  • 2622-08-4

  • 5g

  • 919.0CNY

  • Detail
  • Alfa Aesar

  • (10258)  Tri(o-tolyl) phosphite, typically C 71%, H 6%   

  • 2622-08-4

  • 25g

  • 3380.0CNY

  • Detail

2622-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(2-methylphenyl) phosphite

1.2 Other means of identification

Product number -
Other names Phosphorous acid, tris(2-methylphenyl) 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:2622-08-4 SDS

2622-08-4Relevant articles and documents

Diphenyl Diselenide-Catalyzed Synthesis of Triaryl Phosphites and Triaryl Phosphates from White Phosphorus

Zhang, Yue,Cai, Ziman,Chi, Yangyang,Zeng, Xiangzhe,Chen, Shuanghui,Liu, Yan,Tang, Guo,Zhao, Yufen

supporting information, p. 5158 - 5163 (2021/07/20)

Industrially important triaryl phosphites, traditionally prepared from PCl3, have been synthesized by a diphenyl diselenide-catalyzed one-step procedure involving white phosphorus and phenols, which provides a halogen- and transition metal-free way to these compounds. Subsequent oxidation of triaryl phosphites produces triaryl phosphates and triaryl thiophosphates. Phosphorotrithioates are also prepared efficiently from aromatic thiols and aliphatic thiols.

Simple phosphonic inhibitors of human neutrophil elastase

Sieńczyk, Marcin,Winiarski, ?ukasz,Kasperkiewicz, Paulina,Psurski, Mateusz,Wietrzyk, Joanna,Oleksyszyn, Józef

supporting information; experimental part, p. 1310 - 1314 (2011/04/16)

Herein, we describe the synthesis and resulting activity of a complex series of α-aminophosphonate diaryl esters as irreversible human neutrophil elastase inhibitors and their selectivity preference for human neutrophil elastase over several other serine proteases such as porcine pancreatic elastase, trypsin, and chymotrypsin. We synthesized and examined the inhibitory potency of several new simple Cbz-protected α- aminoalkylphosphonate diaryl esters that yielded several new HNE inhibitors, where one of the obtained compounds Cbz-ValP(OC6H 4-4-COOMe)2 displayed an apparent second-order inhibition value at 33,015 M-1 s-1.

Selective synthesis of organophosphites

-

Page 12-13, (2008/06/13)

Disclosed herein is a process for the selective synthesis of triorganophosphites intermediates, including chloridites and dichloridites, from PX3 (X=Cl, Br or I), alcoholos and triorganoamines where alcohol and triorganoamine are added either (a) separately and concurrently, or (b) alternating equimolar portions of amine and alcohol.

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