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Ethyl 6-oxaspiro[2.5]octane-1-carboxylate is a carboxylate ester with the molecular formula C10H16O3. It features a unique spiro ring structure, which endows it with distinctive properties. This chemical compound is widely utilized in organic synthesis and pharmaceutical research, serving as a valuable building block for the development of various compounds. Its functional group and structural attributes make it particularly advantageous in the creation of pharmaceuticals and other fine chemicals. Careful handling and adherence to safety protocols are essential when working with Ethyl 6-oxaspiro[2.5]octane-1-carboxylate in laboratory environments.

909406-74-2

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909406-74-2 Usage

Uses

Used in Organic Synthesis:
Ethyl 6-oxaspiro[2.5]octane-1-carboxylate is used as a building block in organic synthesis for its unique spiro ring structure and carboxylate functional group, which contribute to the formation of diverse chemical compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, Ethyl 6-oxaspiro[2.5]octane-1-carboxylate is employed as a key intermediate in the synthesis of pharmaceuticals. Its distinctive structural features make it a promising candidate for the development of new drugs and therapeutic agents.
Used in the Creation of Fine Chemicals:
Ethyl 6-oxaspiro[2.5]octane-1-carboxylate is also utilized in the production of fine chemicals due to its unique properties and the versatility it offers in chemical reactions. This makes it a valuable component in various specialized chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 909406-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,4,0 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 909406-74:
(8*9)+(7*0)+(6*9)+(5*4)+(4*0)+(3*6)+(2*7)+(1*4)=182
182 % 10 = 2
So 909406-74-2 is a valid CAS Registry Number.

909406-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-oxaspiro[2.5]octane-1-carboxylate

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:909406-74-2 SDS

909406-74-2Relevant academic research and scientific papers

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

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, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Heterocyclic-substituted alkanamides as therapeutic compounds

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, (2008/12/07)

Use of compounds of the general formula (I) and pharmaceutically acceptable salt thereof, in which R1 and R2 have the definitions illustrated in detail in the description, as beta-secretase, cathepsin D, plasmepsin II and/or HIV protease inhibitors.

5-AMINO-4-HYDROXY-7- (IMIDAZO [1,2-A] PYRIDIN-6- YLMETHYL)-8-METHYL-NONAMIDE DERIVATIVES AND RELATED COMPOUNDS AS RENIN INHIBITORS FOR THE TREATMENT OF HYPERTENSION

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Page/Page column 40-41, (2008/06/13)

Compounds of the general formula (I) or its salt or a compound in which one or more atoms are replaced by their stable, nonradio-active isotopes, in particular its pharmaceutically acceptable salt; in which X is -CH2-; R1 is a mono- to tetrasubstituted, mono- or bicyclic, unsaturated heterocyclic radical having 1 to 4 nitrogen atoms, R2 is C1-6alkyl or C3-6cycloalkyl; R3 is independently of one another H, C1-6alkyl, C1-6alkoxycarbonyl or C1-6alkanoyl; R4 is C2-6alkenyl, C1-6alkyl, unsubstituted or substituted aryl- C1-6alkyl or C3-8cycloalkyl; R5 is -Lm-R6; L is C1-6alkylene which is optionally substituted by 1-4 halogen, or a linker: formula (II) n = 0, 1 or 2; m = 0 or 1; R6 is a radical composed of 2 cyclic systems selected from bicyclo[x.y.z]alkyl, spiro[o.p]alkyl, mono- or bioxabicyclo[x.y.z]alkyl or mono- or bioxaspiro[o.p]alkyl, all of which may be substituted by 1-3 substituents selected from C1-6alkyl, C1-6alkoxy, cyano, halogen, C1-6alkoxy- C1-6alkyl, hydroxy-C1-6alkyl or dialkylamino, or if m = 0: is also saturated C3-8heterocyclyl which comprises 1-2 oxygen atoms, substituted by 1-3 substituents selected from C1-6alkyl, C1-6alkoxy, cyano, halogen, C1-6alkoxy- C1-6alkyl, hydroxy- C1-6alkyl or dialkylamino, or if m = 1: is also saturated C3-8heterocyclyl which comprises 1-2 oxygen atoms, optionally substituted by 1-3 substituents selected from C1-6alkyl, C1-6alkoxy, cyano, halogen, C1-6-alkoxy-C1-6alkyl, hydroxy-C1-6alkyl or dialkylamino; have renin- inhibiting properties and can be used as medicines for the treatment of hypertension.

HETEROCYCLIC-SUBSTITUTED ALKANAMIDES USEFUL AS RENIN INHIBITORS

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Page/Page column 30-31, (2010/11/23)

Compounds of the general formula (I) in which the meanings of the substituents R1 and R2 are as stated in claim 1, have renin-inhibiting properties and can be used as medicines.

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