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15753-47-6

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15753-47-6 Usage

General Description

1-(Hydroxymethyl)cyclohexanol is a chemical compound with the molecular formula C7H14O2. It is a cyclohexane derivative with a hydroxymethyl substituent, and can exist as different isomers. 1-(hydroxymethyl)cyclohexanol is commonly used in organic synthesis as a building block for the production of pharmaceuticals, agrochemicals, and other fine chemicals. It can also be used as a solvent or in the formulation of personal care products. Additionally, 1-(hydroxymethyl)cyclohexanol has potential applications in the development of new materials and polymers due to its unique structural properties. However, it is important to handle this chemical with care as it may pose certain health and safety risks if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 15753-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,5 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15753-47:
(7*1)+(6*5)+(5*7)+(4*5)+(3*3)+(2*4)+(1*7)=116
116 % 10 = 6
So 15753-47-6 is a valid CAS Registry Number.

15753-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(hydroxymethyl)cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names hydroxymethyl cyclohexanol

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:15753-47-6 SDS

15753-47-6Relevant articles and documents

N-(chloromethyloxycarbonyl)pyrrolidine as a source of the HOCH2- synthon

Guijarro, Albert,Yus, Miguel

, p. 5593 - 5596 (1996)

The reaction of N-(chloromethyloxycarbonyl)pyrrolidine (1) with lithium powder and a catalytic amount of DTBB (2.5 mol %) in the presence of different electrophiles [Me3SiCl, Bu(i)CHO, Bu(t)CHO, PhCHO, Et2CO, (CH2)5CO, PhCOMe, Ph2CO] in THF at -78°C leads, after hydrolysis with water, to the expected functionalised carbamates 2. Deprotection of the acetophenone derivative 2g with DIBALH at THF reflux yields, after hydrolysis, the corresponding 1,2-diol 3g.

Selective transition-metal-free vicinal cis-dihydroxylation of saturated hydrocarbons

Bering, Luis,Antonchick, Andrey P.

, p. 452 - 457 (2016/12/30)

A transition-metal-free cis-dihydroxylation of saturated hydrocarbons under ambient reaction conditions has been developed. The described approach allows a direct and selective synthesis of vicinal diols. The new reaction thereby proceeds via radical iodination and a sequence of oxidation steps. A broad scope of one-pot dual C(sp3)-H bond functionalization for the selective synthesis of vicinal syn-diols was demonstrated.

Mild deprotection of methylene acetals in combination with trimethylsilyl triflate-2,2′-bipyridyl

Fujioka, Hiromichi,Senami, Kento,Kubo, Ozora,Yahata, Kenzo,Minamitsuji, Yutaka,Maegawa, Tomohiro

experimental part, p. 426 - 428 (2011/02/26)

The facile deprotection of methylene acetal protection of diols under mild conditions is established. The combination of trimethylsilyl triflate (TMSOTf) and 2,2′-bipyridyl followed by a weakly acidic hydrolysis was effective and the substrates having acid sensitive functional groups can be tolerated under the stated conditions. The selective deprotection between methylene acetal and benzophenone ketal was achieved.

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