Welcome to LookChem.com Sign In|Join Free
  • or
3aH-Cyclopent[d]isoxazole-3a-methanol, hexahydro-2-methyl-3-propyl, (3R,3aR,6aR)-(9CI) is a complex organic compound with a unique molecular structure. It is a derivative of cyclopentane, featuring an isoxazole ring and a hydroxyl group. The compound is characterized by its hexahydro nature, indicating the presence of six hydrogen atoms in a cyclic structure. The 2-methyl and 3-propyl substituents contribute to its steric properties, with the 2-methyl group attached to the second carbon and the 3-propyl group attached to the third carbon. The stereochemistry is defined by the (3R,3aR,6aR) configuration, which specifies the spatial arrangement of the atoms at these positions. 3aH-Cyclopent[d]isoxazole-3a-methanol,hexahydro-2-methyl-3-propyl-,(3R,3aR,6aR)-(9CI) is of interest in the field of organic chemistry, potentially for its pharmaceutical or chemical properties, although specific applications are not detailed in the provided information.

607405-12-9

Post Buying Request

607405-12-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

607405-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 607405-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,4,0 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 607405-12:
(8*6)+(7*0)+(6*7)+(5*4)+(4*0)+(3*5)+(2*1)+(1*2)=129
129 % 10 = 9
So 607405-12-9 is a valid CAS Registry Number.

607405-12-9SDS

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 3aH-Cyclopent[d]isoxazole-3a-methanol,hexahydro-2-methyl-3-propyl-,(3R,3aR,6aR)-(9CI)

1.2 Other means of identification

Product number -
Other names -

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:607405-12-9 SDS

607405-12-9Downstream Products

607405-12-9Relevant academic research and scientific papers

Organocatalysts promote enantioselective 1,3-dipolar cycloadditions of nitrones with 1-cycloalkene-1-carboxaldehydes

Karlsson, Staffan,Hoegberg, Hans-Erik

, p. 2782 - 2791 (2007/10/03)

In the presence of enantiopure organocatalysts, 1-cycloalkene-1-carboxaldehydes and various nitrones furnished fused isoxazolidines. Thus, some chiral pyrrolidinium salts catalyzed the formation of such cycloadducts in high diastereoand enantioselectivity (up to 92% ee). The predominant diastereomer, the exo one, was mostly obtained in excellent diastereoselectivity (> 99:1 dr). Furthermore, after recrystallization of one of the cycloadducts, this was obtained enantiomerically pure (> 99% ee). The absolute configuration of one of the cycloadducts was determined. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 607405-12-9