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1,2-Propanediol, 3-(4-iodophenoxy)-, also known as 3-(4-iodophenoxy)propane-1,2-diol or 4-iodophenoxypropane-1,2-diol, is an organic compound with the chemical formula C9H11IO3. It is a colorless to pale yellow liquid with a molecular weight of 292.09 g/mol. 1,2-Propanediol, 3-(4-iodophenoxy)- is characterized by the presence of a propanediol backbone, with a 4-iodophenoxy group attached to the third carbon. It is used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other bioactive compounds. Due to its reactivity and potential applications, it is important to handle 1,2-Propanediol, 3-(4-iodophenoxy)- with care, following appropriate safety guidelines.

830-11-5

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830-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 830-11-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 830-11:
(5*8)+(4*3)+(3*0)+(2*1)+(1*1)=55
55 % 10 = 5
So 830-11-5 is a valid CAS Registry Number.

830-11-5Downstream Products

830-11-5Relevant academic research and scientific papers

Synthesis and self-assembly of 5,5′-bis(phenylethynyl)-2,2′-bithiophene-based bolapolyphiles in triangular and square LC honeycombs

Gao, Hongfei,Cheng, Huifang,Yang, Zonghan,Prehm, Marko,Cheng, Xiaohong,Tschierske, Carsten

, p. 1301 - 1308 (2015/02/19)

A series of X-shaped 5,5′-bis(phenylethynyl)-2,2′-bithiophene-based bolaamphiphiles bearing two long lateral alkyl chains and two terminal glycerol groups has been synthesized by using Kumada and Sonogashira coupling reactions as key steps. The thermotropic liquid crystalline behavior of these compounds was investigated by POM, DSC and X-ray scattering. With elongation of the lateral alkyl chains two different kinds of liquid crystalline phases with honeycomb structures, ColhexΔ/p6mm, formed by (defective) triangular honeycomb cells, and Colsqu/p4mm with square cells were observed for these compounds. UV and PL measurements indicate fluorescent properties making them potential candidates for application in fluorescence sensor devices.

Triblock polyphiles through click chemistry: Self-assembled thermotropic cubic phases formed by micellar and monolayer vesicular aggregates

Tan, Xiaoping,Kong, Leiyang,Dai, Heng,Cheng, Xiaohong,Liu, Feng,Tschierske, Carsten

, p. 16303 - 16313 (2013/12/04)

Three series of triblock polyphiles consisting of a rigid 4-phenyl-1,2,3-triazole or 1,4-diphenyl-1,2,3-triazole core with three lipophilic and flexible alkoxyl chains at one end and a polar glycerol group at the opposite end were synthesized by copper-ca

Cyclic sulfites, key intermediates in synthesis of 1-alkylamino-3-aryloxy-2-propanols from glycidol

Bredikhina,Savel'ev,Bredikhin

, p. 213 - 219 (2007/10/03)

A number of 3-aryloxypropanedioles were obtained by treating glycidol with phenols. The latter with thionyl chloride afforded 4-aryloxymethyl-1,3,2-dioxathiolane 2-oxides. These compounds were also obtained from 4-chloromethyl-1,3,2-dioxathiolane 2-oxides by substitution aryloxy group for chlorine. The cyclic sulfides synthesized are universal intermediates in the synthesis of chiral aryloxypropanolamines among which are known β-adrenoblockaders, cardiovascular drugs. From (S)-glycidol, (S)-alprenolol, (S)-propanolol, and (S)-thymolol were synthesized.

Compounds having one or more aminosulfaonyloxy radicals useful as pharmaceuticals

-

, (2008/06/13)

Methods of treating chronic arthritis and osteoporosis which utilize both known and novel compounds which would fall under the general formula:(HO)p--A--[--OS(O) 2 NR 1 R 2 ] zwherein A encompasses a wide range of values including but not limited to aryl, loweralkyl, cycloalkyl, and carbohydrates including sucrose and fructose; p is equal to the number of unreacted hydroxy groups contained on the molecule and may be zero; z is the number of --OS(O) 2 NR 1 R 2 groups and is always at least one; R 1 and R 2 are selected from hydrogen, loweralkyl, carboxy and the like; a novel process for preparing the compounds is provided wherein an appropriate sulfamic acid aryl ester is reacted with a hydroxy substituted A radical which may or may not contain thereon protected carboxyl, amino or hydroxy substituents, in an aprotic solvent containing a tertiary amine base. Pharmaceutical compositions for the treatment of chronic arthritis and osteoporosis are also provided.

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