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14064-13-2

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14064-13-2 Usage

Description

1-HYDROXYMETHYL-1-METHYLCYCLOHEXANE, also known as 1-Hydroxymethyl-1-methylcyclohexane, is an organic compound with the chemical formula C8H16O. It is a pale yellow oil at room temperature and is primarily used in organic synthesis due to its unique chemical structure.

Uses

Used in Organic Synthesis:
1-HYDROXYMETHYL-1-METHYLCYCLOHEXANE is used as a synthetic building block for the creation of various organic compounds. Its unique structure allows it to be a versatile intermediate in the synthesis of a wide range of chemical products, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Pharmaceutical Industry:
1-HYDROXYMETHYL-1-METHYLCYCLOHEXANE is used as a key intermediate in the development of new pharmaceutical compounds. Its chemical properties make it suitable for the synthesis of various drug molecules, contributing to the advancement of novel treatments for various medical conditions.
Used in Agrochemical Industry:
1-HYDROXYMETHYL-1-METHYLCYCLOHEXANE is used as a starting material in the synthesis of agrochemicals, such as pesticides and herbicides. Its application in this industry helps in the development of more effective and environmentally friendly products for agricultural use.
Used in Specialty Chemicals Industry:
1-HYDROXYMETHYL-1-METHYLCYCLOHEXANE is used as a raw material in the production of specialty chemicals, which are high-value chemicals used in various applications, such as coatings, adhesives, and sealants. Its unique properties make it an essential component in the formulation of these high-performance materials.

Check Digit Verification of cas no

The CAS Registry Mumber 14064-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14064-13:
(7*1)+(6*4)+(5*0)+(4*6)+(3*4)+(2*1)+(1*3)=72
72 % 10 = 2
So 14064-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-8(7-9)5-3-2-4-6-8/h9H,2-7H2,1H3

14064-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-methylcyclohexyl)methanol

1.2 Other means of identification

Product number -
Other names Cyclohexanemethanol,1-methyl

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:14064-13-2 SDS

14064-13-2Relevant articles and documents

Preparation of isoquinazolines: Via metal-free [4 + 2] cycloaddition of ynamides with nitriles

Wu, Hao,Liu, Yu,He, Ming-Xing,Wen, Hao,Cao, Wei,Chen, Ping,Tang, Yu

, p. 8408 - 8416 (2019/09/30)

TfOH-mediated [4 + 2] cycloaddition of ynamides with nitriles to construct 1,2-dihydroquinazolines is realized by a direct reaction in moderate to excellent yields (up to 93%) in a stereospecific manner. A rapid and efficient strategy has been employed for the syntheses of alkyl-substituted 1,2-dihydroquinazoline derivatives, and it exhibits good functional group tolerance, has a short reaction time, shows excellent diastereoselectivity, and is a simple and high-yielding reaction.

Hemilabile Benzyl Ether Enables γ-C(sp3)-H Carbonylation and Olefination of Alcohols

Tanaka, Keita,Ewing, William R.,Yu, Jin-Quan

supporting information, (2019/10/22)

Pd-catalyzed C(sp3)-H activation of alcohol typically shows β-selectivity due to the required distance between the chelating atom in the attached directing group and the targeted C-H bonds. Herein we report the design of a hemilabile directing group which exploits the chelation of a readily removable benzyl ether moiety to direct γ- or δ-C-H carbonylation and olefination of alcohols. The utility of this approach is also demonstrated in the late-stage C-H functionalization of β-estradiol to rapidly prepare desired analogues that required multi-step syntheses with classical methods.

CYCLOALKYL METHOXYBENZYL PHENYL PYRAN DERIVATIVES AS SODIUM DEPENDENT GLUCOSE CO TRANSPORTER (SGLT2) INHIBITORS

-

, (2012/03/26)

The invention relates to the cycloalkyl methoxybenzyl phenyl pyran derivatives as Sodium dependent glucose co transporter (SGLT) inhibitors, particularly SGLT2 and method of treating diseases, conditions and/or disorders inhibited by SGLT2 with them, and processes for preparing them.

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