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86111-47-9

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86111-47-9 Usage

General Description

Benzenemethanol, 2,6-dichloro-4-methoxy- is a chemical compound with the molecular formula C8H7Cl2O2. It is also known as 2,6-dichloro-4-methoxybenzyl alcohol. Benzenemethanol, 2,6-dichloro-4-methoxy- is a white solid with a faint odor and is slightly soluble in water. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a reagent in organic chemical reactions. The compound can be hazardous if ingested, inhaled, or comes into contact with the skin, and proper safety precautions should be taken when handling it.

Check Digit Verification of cas no

The CAS Registry Mumber 86111-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,1 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86111-47:
(7*8)+(6*6)+(5*1)+(4*1)+(3*1)+(2*4)+(1*7)=119
119 % 10 = 9
So 86111-47-9 is a valid CAS Registry Number.

86111-47-9Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS FOR HISTONE LYSINE DEMETHYLASE INHIBITION

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Paragraph 0737; 0765, (2022/03/09)

The present disclosure relates generally to compounds and pharmaceutical compositions for the selective inhibition of histone lysine demethylase5 (KDM5), particularly KDM5B, and methods of their use in treating conditions and diseases associated with KDM5 activity.

GUANIDINOBENZOIC ACID COMPOUND

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Paragraph 0144, (2014/08/06)

[Problem] Provided is a compound which is useful as an agent for preventing and/or treating renal diseases. [Means for Solution] The present inventors have conducted extensive studies on compounds having a trypsin inhibitory action, and as a result, they

Synthesis of novel structurally simplified estrogen analogues with electron-donating groups in ring A

Tietze, Lutz F.,Vock, Carsten A.,Krimmelbein, Ilga K.,Nacke, Linda

experimental part, p. 2040 - 2060 (2009/12/27)

A library of 25 novel estrogen analogues were prepared in five to eight steps from mostly commercially available substituted anisoles via bromination, formylation, Corey-Fuchs reaction, elimination, and Sonogashira reaction. Georg Thieme Verlag Stuttgart.

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