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1-Oxaspiro[2.5]octane, 6-methyl- is a cyclic organic compound characterized by a unique spiro structure, which consists of a six-membered ring fused to a five-membered oxaspiro ring. The compound is further defined by the presence of a methyl group at the 6th carbon position. It is a colorless liquid with a molecular formula of C9H16O and a molecular weight of 140.22 g/mol. 1-Oxaspiro[2.5]octane, 6-methyl- is primarily used as a synthetic intermediate in the production of various pharmaceuticals and agrochemicals, owing to its potential to form complex molecular architectures. Its chemical properties and reactivity make it a valuable building block in organic synthesis, particularly in the creation of molecules with specific biological activities.

38709-71-6

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38709-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38709-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,0 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38709-71:
(7*3)+(6*8)+(5*7)+(4*0)+(3*9)+(2*7)+(1*1)=146
146 % 10 = 6
So 38709-71-6 is a valid CAS Registry Number.

38709-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-1-oxaspiro[2.5]octane

1.2 Other means of identification

Product number -
Other names 6-methyl-1-oxa-spiro[2.5]octane

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:38709-71-6 SDS

38709-71-6Relevant academic research and scientific papers

Stereochemical preference of yeast epoxide hydrolase for the O-axial C3 epimers of 1-oxaspiro[2.5]octanes

Weijers, Carel A. G. M.,Koenst, Paul M.,Franssen, Maurice C. R.,Sudhoelter, Ernst J. R.

, p. 3106 - 3114 (2007)

The 1-oxaspiro[2.5]octane moiety is a common motif in many biologically active spiroepoxide compounds. Stereochemistry plays an important role in the action of these spiroepoxides, since the O-axial C3 epimers are predominantly responsible for biological

OXYSTEROLS AND METHODS OF USE THEREOF

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Paragraph 00462, (2018/05/16)

Compounds are provided according to Formula (I): and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof; wherein R2, R3, R4, R5, and and R6 are as defined herein. Compounds of the present invention are contemplated useful for the prevention and treatment of a variety of conditions.

Revisiting the Corey-Chaykovsky reaction: The solvent effect and the formation of β-hydroxy methylthioethers

Peng, Yu,Yang, Jin-Hui,Li, Wei-Dong Z.

, p. 1209 - 1215 (2007/10/03)

The classical Corey-Chaykovsky (CC) reaction of ketones in ethereal solvents (i.e., THF or Et2O) resulted in the production of a significant amount of β-hydroxy methylthioether 2 along with normal epoxide product 1. Some interesting and synthet

EPOXIDE FORMATION FROM ALDEHYDES AND KETONES - A MODIFIED METHOD FOR PREPARING THE COREY-CHAYKOVSKY REAGENTS

Ng, John S.

, p. 1193 - 1202 (2007/10/02)

Trimethylsulfoxonium iodide and potassium tert-butoxide in dimethyl sulfoxide (DMSO) is a very efficient process for the multikilogram scale preparation of epoxides from aldehydes and ketones.

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