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Ethyl 5-hydroxy-2-iodobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99665-70-0

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99665-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99665-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,6 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99665-70:
(7*9)+(6*9)+(5*6)+(4*6)+(3*5)+(2*7)+(1*0)=200
200 % 10 = 0
So 99665-70-0 is a valid CAS Registry Number.

99665-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-hydroxy-2-iodobenzoate

1.2 Other means of identification

Product number -
Other names ethyl 5-hydroxy-2-hexynoate

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:99665-70-0 SDS

99665-70-0Relevant academic research and scientific papers

Preparation of soluble and insoluble polymer supported IBX reagents.

Reed, Neal N,Delgado, Mercedes,Hereford, Kristina,Clapham, Bruce,Janda, Kim D

, p. 2047 - 2049 (2007/10/03)

A series of soluble and insoluble polymer supported versions of the versatile oxidizing reagent IBX has been prepared. Each of the reagents were evaluated for their efficiency in the conversion of benzyl alcohol to benzaldehyde. Results from this study were that the soluble, non-crosslinked polystyrene supported IBX reagent gave the best rate of conversion to benzaldehyde, while the macroporous polymer supported IBX resin provided a superior rate of conversion to benzaldehyde when compared with a gel type resin. The macroporous IBX reagent was also shown to convert a series of alcohols to the corresponding aldehydes and ketones.

Efficient Catalytic Cleavage of Reactive Phosphates by an o-Iodosobenzoate Functionalized Surfactant

Moss, Robert A.,Kim, Kwang Yoo,Swarup, Shanti

, p. 788 - 793 (2007/10/02)

5-(N-(n-Hexadecyl)-N,N-dimethyl-N-(β-ethyloxy)ammonium)-2-iodosobenzoate, 1c, cleaved p-nitrophenyl diphenyl phosphate (PNPDPP), p-nitrophenyl diethyl phosphate (PNPDEP), and p-nitrophenyl isobutyl methylphosphonate (PNPIMP) in aqueous cetyltrimethylammonium chloride (CTACl) at pH 8 and 25 deg C.With 4E-5 M 1c in 2E-4 M CTACl, second-order cleavage rate constants (L/(M-s)) were PNPDPP, 28 500, PNPDEP, 0.865, and PNPIMP, 215.These represented kinetic advantages of 14700, 43600 and 846, respectively, over nonfunctional CTACl-catalyzed cleavages of the substrates.In the presence of excess PNPDPP at pH 8, catalyst 1c/CTACl "turned over" with k ca. 0.17 s-1 for the hydrolysis of the putative 1c-diphenyl phosphate intermediate.

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