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1,4-Dioxaspiro[4.6]undec-6-ene is a bicyclic dioxaspiro compound with the molecular formula C11H16O2. It features a unique spiro ring structure that endows it with distinctive chemical and physical properties. Known for its pleasant odor and stability, this chemical compound is commonly synthesized through organic chemical reactions and is widely used in the formulation of fragrances and as a chemical intermediate in the production of various other compounds.

1728-24-1

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1728-24-1 Usage

Uses

Used in Fragrance Industry:
1,4-Dioxaspiro[4.6]undec-6-ene is used as a fragrance ingredient for its pleasant odor, contributing to the creation of various scent profiles in perfumes, cosmetics, and other fragranced products.
Used in Chemical Industry:
1,4-Dioxaspiro[4.6]undec-6-ene serves as a chemical intermediate, playing a crucial role in the synthesis of other compounds for various applications across different industries.
It is important to handle 1,4-Dioxaspiro[4.6]undec-6-ene with care, as it may pose potential health hazards if not used and stored properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1728-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1728-24:
(6*1)+(5*7)+(4*2)+(3*8)+(2*2)+(1*4)=81
81 % 10 = 1
So 1728-24-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-2-4-6-9(5-3-1)10-7-8-11-9/h3,5H,1-2,4,6-8H2

1728-24-1SDS

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 1,4-dioxaspiro[4.6]undec-6-ene

1.2 Other means of identification

Product number -
Other names 2-Cyclohepten-1-on-aethylenketal

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:1728-24-1 SDS

1728-24-1Relevant articles and documents

CERTAIN FUSED PYRROLECARBOXAMIDES A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS

-

, (2008/06/13)

Disclosed are compounds of formula I: STR1 wherein R 8 and R. sub.9 independently represent hydrogen or organic substituents; W represents optionally substituted thiazolyl or quinoxalinyl; X is hydrogen, hydroxy or lower alkyl; andT is hydrogen, halogen, hydroxy, nitro, amino or alkyl,which compounds are highly selective agonists, antagonists or inverse agonists for GABAa brain receptors or prodrugs of agonists, antagonists or inverse agonists for GABAa brain receptor. These compounds are useful in the diagnosis and treatment of anxiety, sleep and seizure disorders, overdose with benzodiazepine drugs and for enhancement of memory.

CERTAIN PYRROLO PYRIDINE-3-CARBOXAMIDES; A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS

-

, (2008/06/13)

The present invention encompasses structures of the formula: STR1 or the pharmaceutically acceptable non-toxic salts thereof wherein: STR2 wherein: W represents substituted or unsubstituted phenyl;X is hydrogen, hydroxy or lower alkyl; T is hydrogen, halogen, hydroxy, nitro, amino or alkyl; R. sub.3 is hydrogen or an organic group;R 4 is hydrogen or substituted or unsubstituted organic substituent;R 5 and R 6 represent organic, and inorganic substituents; andn is 1, 2, 3, or 4, which compounds are highly selective agonists, antagonists or inverse agonists for GABAa brain receptors or prodrugs of agonists, antagonists or inverse agonists for GABAa brain receptors. These compounds are useful in the diagnosis and treatment of anxiety, sleep and seizure disorders, overdose with benzodiazepine drugs and for enhancement of memory.

Synthetic studies on the 1-hydroxy nortropane system: An approach to Calystegines.

Ducrot, P.-H.,Beauhaire, J.,Lallemand, J. Y.

, p. 3883 - 3886 (2007/10/02)

A general synthetic strategy for 1-hydroxy nortropane skeleton, the common feature of calystegines is described.

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