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2-benzyloxy-6-(1-hydroxyethyl)naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136241-83-3

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136241-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136241-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136241-83:
(8*1)+(7*3)+(6*6)+(5*2)+(4*4)+(3*1)+(2*8)+(1*3)=113
113 % 10 = 3
So 136241-83-3 is a valid CAS Registry Number.

136241-83-3Downstream Products

136241-83-3Relevant academic research and scientific papers

Optically active naphthalene derivative, process for preparation thereof, liquid crystal composition containing the same as effective component, and liquid crystal element using the same

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, (2008/06/13)

Optically active naphthalene derivatives including optically active naphthylcarboxylic acid derivative, hydroxynaphthalene derivative, alkoxynaphthylalkanol derivative and alkylnaphthylalkanol derivative have the following structural formula: STR1 wherein R1 denotes an alkyl group of 3-20 carbon atoms, R2 denotes an alkyl group of 1-20 carbon atoms optionally substituted with halogen atom(s) or an alkoxyalkyl group of 2-20 carbon atoms optionally substituted with halogen atom(s), X denotes --COO-- or --OCO--, k, l and m denotes 0 or 1 respectively, n denotes an integer of 0-6, p denotes 0 or 1, and the asterisk indicates an asymmetric carbon atom, with the proviso that when k is 0, l and m are not 1 at the same time, and when k is 1, m is 1, and when n is 0 and m is 1, X is --COO--. These optically active naphthalene derivatives are useful as a ferroelectric liquid crystal materials or its component having a sufficient spontaneous polarization and by which a high speed response is possible and which further exhibits a ferroelectric liquid crystal phase in a temperature region around room temperature. Processes for the preparation of the optically active derivatives are also disclosed.

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