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436865-00-8

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436865-00-8 Usage

General Description

1-Hexanol, 6-(4-iodophenoxy)- is a chemical compound with the molecular formula C12H17IO2. It is a derivative of 1-hexanol, with an added 4-iodophenoxy group. This chemical is used in organic synthesis and research applications, particularly in the preparation of various compounds for pharmaceutical and agrochemical industries. It may also have potential applications in the development of new materials or as a building block for the synthesis of other organic compounds. As with any chemical compound, proper handling and safety precautions should be taken when working with 1-Hexanol, 6-(4-iodophenoxy)- to ensure the health and safety of those handling it.

Check Digit Verification of cas no

The CAS Registry Mumber 436865-00-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,8,6 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 436865-00:
(8*4)+(7*3)+(6*6)+(5*8)+(4*6)+(3*5)+(2*0)+(1*0)=168
168 % 10 = 8
So 436865-00-8 is a valid CAS Registry Number.

436865-00-8Relevant articles and documents

POLYMERIZABLE COMPOUND AND OPTICAL ANISOTROPIC BODY

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Paragraph 0155-0156, (2016/10/08)

PROBLEM TO BE SOLVED: To provide a polymerizable compound that has a high refractive index anisotropy, prevents the occurrence of crystal deposition or the like when added to a polymerizable liquid crystal composition and has high storage stability, also

Synthesis of d-glucose and l-phenylalanine substituted phenylene-thiophene oligomers

Hassan Omar, Omar,Babudri, Francesco,Farinola, Gianluca M.,Naso, Francesco,Operamolla, Alessandra,Pedone, Adriana

experimental part, p. 486 - 494 (2011/03/18)

Phenylene-thiophene oligomers bearing peracetylated β-d-glucose or N-BOC-l-phenylalanine as chiral substituents were synthesized in good yields by a versatile protocol based on the Suzuki-Miyaura cross-coupling reaction. Aryl iodides bearing the chiral bi

Controlled homeotropic and homogeneous orientations for nanoscale phase-separated domain of light-emitting amphiphilic block copolymer bearing a 2,5-diarylthiazole moiety

Mori, Atsunori,Shikuma, Junichi,Kinoshita, Motoi,Ikeda, Tomiki,Misaki, Masahiro,Ueda, Yasukiyo,Komura, Motonori,Asaoka, Sadayuki,Iyoda, Tomokazu

, p. 272 - 273 (2008/09/20)

An amphiphilic block copolymer composed of poly(ethylene oxide) and poly(methacrylate ester) bearing a donor-acceptor-type 2,5-diarylthiazole in the side chain is prepared by atom-transfer radical polymerization. The precursor 2,5-diarylthiazole monomer i

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