Welcome to LookChem.com Sign In|Join Free

CAS

  • or

45982-66-9

Post Buying Request

45982-66-9 Suppliers

Recommended suppliersmore

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

45982-66-9 Usage

Molecular structure

1,4-Dioxaspiro[4.5]decane-2-methanamine has a complex molecular structure with two fused rings (a spiro compound) that share a single atom.

Derivative of spiro compounds

This chemical compound is derived from spiro compounds, which are known for their unique structure and properties.

Amine functional group

The presence of the amine functional group (-NH2) indicates that the compound contains a nitrogen atom, which can affect its reactivity and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 45982-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,9,8 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 45982-66:
(7*4)+(6*5)+(5*9)+(4*8)+(3*2)+(2*6)+(1*6)=159
159 % 10 = 9
So 45982-66-9 is a valid CAS Registry Number.

45982-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dioxaspiro[4.5]decan-3-ylmethanamine

1.2 Other means of identification

Product number -
Other names F2189-0240

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:45982-66-9 SDS

45982-66-9Relevant articles and documents

N-Hydroxyl derivatives of guanidine based drugs as enzymatic NO donors

Xian, Ming,Li, Xiaopeng,Tang, Xiaoping,Chen, Xinchao,Zheng, Zhongling,Galligan, James J,Kreulen, David L,Wang, Peng G

, p. 2377 - 2380 (2007/10/03)

Recent research suggests that NO may play a role in the physiological effects of some guanidine-containing drugs. In this report, three guanidine-containing drugs (guanadrel, guanoxan, and guanethidine) together with their N-hydroxyl derivatives were synthesized and their NO-releasing abilities catalyzed by nitric oxide synthases (NOSs) and horseradish peroxidase were evaluated. The guanidine containing compounds could not release NO in the presence of NOS or peroxidase. The corresponding N-hydroxyl compounds exhibited weak NO-releasing ability under the catalyzed of NOS and good NO-releasing ability under the oxidation by horseradish peroxidase in the presence of H2O2. These compounds also displayed vasodilatory activity. Elsevier Science Ltd. All rights reserved.

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

What can I do for you?
Get Best Price

Get Best Price for 45982-66-9