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134136-04-2

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134136-04-2 Usage

General Description

(1,4-Dioxa-spiro[4.5]dec-8-yl)-acetic acid is a unique chemical compound that consists of a spiro (bridged) ring structure with two oxygen atoms and an acetic acid functional group. (1,4-Dioxa-spiro[4.5]dec-8-yl)-acetic acid is not commonly found in nature and is mostly synthesized in the laboratory for research and industrial purposes. Its specific properties and uses are not well-documented, but it may have potential applications in pharmaceuticals, organic synthesis, and materials science due to its unusual structure and reactivity. Further research and experimentation are needed to fully understand the potential uses and effects of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 134136-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,3 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134136-04:
(8*1)+(7*3)+(6*4)+(5*1)+(4*3)+(3*6)+(2*0)+(1*4)=92
92 % 10 = 2
So 134136-04-2 is a valid CAS Registry Number.

134136-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,4-dioxaspiro[4.5]decan-8-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (1,4-Dioxaspiro[4.5]dec-8-yl)-acetic acid

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:134136-04-2 SDS

134136-04-2Relevant articles and documents

Pd-Catalyzed Highly Chemo- And Regioselective Hydrocarboxylation of Terminal Alkyl Olefins with Formic Acid

Ren, Wenlong,Chu, Jianxiao,Sun, Fei,Shi, Yian

supporting information, p. 5967 - 5970 (2019/08/26)

An efficient Pd-catalyzed hydrocarboxylation of alkenes with HCOOH is described. A wide variety of linear carboxylic acids bearing various functional groups can be obtained with excellent chemo- and regioselectivities under mild reaction conditions. The reaction process is operationally simple and requires no handling of toxic CO.

Synthesis and evaluation of [(1R)-1-amino-2-(2,5-difluorophenyl)ethyl] cyclohexanes and 4-[(1R)-1-amino-2-(2,5-difluorophenyl)ethyl]piperidines as DPP-4 inhibitors

Chen, Ping,Caldwell, Charles G.,Ashton, Wallace,Wu, Joseph K.,He, Huaibing,Lyons, Kathryn A.,Thornberry, Nancy A.,Weber, Ann E.

scheme or table, p. 1880 - 1886 (2011/05/05)

A series of 4-amino cyclohexanes and 4-substituted piperidines were prepared and evaluated for inhibition of DPP-4. Analog 20q displayed both good DPP-4 potency and selectivity against other proteases, while derivative 20k displayed long half life and mod

INHIBITORS OF SERINE PROTEASES FOR THE TREATMENT OF HCV INFECTIONS

-

Page/Page column 472, (2008/12/07)

The present invention relates to compounds of formula (I): or a pharmaceutically acceptable salt thereof. These compounds inhibit serine protease, particularly the hepatitis C virus NS3-NS4A protease.

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