Cas 33472-10-5,diisopropyl ((5-bromo-2-hydroxyphenyl)(hydroxy)methyl)phosphonate

33472-10-5

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Basic information

Product Name: diisopropyl ((5-bromo-2-hydroxyphenyl)(hydroxy)methyl)phosphonate
Synonyms: diisopropyl ((5-bromo-2-hydroxyphenyl)(hydroxy)methyl)phosphonate
CAS NO:33472-10-5
Molecular Formula:
Molecular Weight: 367.177
EINECS: N/A
Product Categories: N/A
Mol File: 33472-10-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: diisopropyl ((5-bromo-2-hydroxyphenyl)(hydroxy)methyl)phosphonate(CAS DataBase Reference)
NIST Chemistry Reference: diisopropyl ((5-bromo-2-hydroxyphenyl)(hydroxy)methyl)phosphonate(33472-10-5)
EPA Substance Registry System: diisopropyl ((5-bromo-2-hydroxyphenyl)(hydroxy)methyl)phosphonate(33472-10-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 33472-10-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 33472-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,7 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33472-10:
(7*3)+(6*3)+(5*4)+(4*7)+(3*2)+(2*1)+(1*0)=95
95 % 10 = 5
So 33472-10-5 is a valid CAS Registry Number.

33472-10-5Upstream product

33472-10-5Downstream Products

33472-10-5Relevant articles and documents

Phospho sulfonic acid: An efficient and recyclable solid acid catalyst for the solvent-free synthesis of α-hydroxyphosphonates and their anticancer properties

Kalla, Reddi Mohan Naidu,Lee, Hye Ri,Cao, Jiafu,Yoo, Jin-Wook,Kim, Il

, p. 3916 - 3922 (2015/05/20)

As a means of developing biologically active compounds, a series of α-hydroxyphosphonates, ArC(OH)PO(OR)2 (Ar = 5-G-2-OHPh; R = Me, Et, iPr, Bu; G = H, Br, Cl, NO2), have been synthesized by reacting diversely substituted salicylalde

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