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130129-10-1

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130129-10-1 Usage

Description

(R)-6-BENZYLOXYMETHYL-4-METHYL-5,6-DIHYDRO-PYRAN-2-ONE, also known as EBXS-4, is a chemical compound that belongs to the class of pyranones. It is defined by its unique structure, which includes a pyran ring with a benzyl and a methyl substituent. EBXS-4 has garnered attention for its potential pharmacological activities, particularly as an inhibitor of enzymes that play a role in various biological processes. Its applications extend to the development of pharmaceuticals and agrochemicals, and it is also used as a synthetic intermediate in organic chemistry for creating other compounds.

Uses

Used in Pharmaceutical Development:
EBXS-4 is used as a potential therapeutic agent for targeting specific enzymes involved in various diseases. Its application in this field is due to its ability to inhibit enzymes, which can lead to the development of new treatments for a range of conditions.
Used in Agrochemical Development:
In the agrochemical industry, EBXS-4 is used as a compound for developing new products that can help control pests and diseases in agriculture. Its role as an enzyme inhibitor makes it a promising candidate for creating targeted and effective solutions.
Used as a Synthetic Intermediate in Organic Chemistry:
EBXS-4 is utilized as a synthetic intermediate for the preparation of various other compounds in organic chemistry. Its unique structure allows for the creation of a wide range of molecules, making it a valuable asset in the synthesis of new chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 130129-10-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,2 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130129-10:
(8*1)+(7*3)+(6*0)+(5*1)+(4*2)+(3*9)+(2*1)+(1*0)=71
71 % 10 = 1
So 130129-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O3/c1-11-7-13(17-14(15)8-11)10-16-9-12-5-3-2-4-6-12/h2-6,8,13H,7,9-10H2,1H3/t13-/m1/s1

130129-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-4-methyl-2-(phenylmethoxymethyl)-2,3-dihydropyran-6-one

1.2 Other means of identification

Product number -
Other names (R)-6-benzyloxymethyl-4-methyl-5,6-dihydro-2H-pyran-2-one

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:130129-10-1 SDS

130129-10-1Relevant articles and documents

Optically active compounds and intermediates thereof, and process for manufacturing same

-

, (2008/06/13)

An optically active (S)- or (R)-pentane compound of the general formula (11): STR1 wherein R11, R12 and R13 independently represent a hydrogen atom or a lower alkyl group having 1 to 4 carbon atoms, R14 represents a hydroxy, protected hydroxy or oxo group, if R14 is an oxo group, the ring denoting benzene in the above formula (11) is benzoquinone, R15 represents a hydrogen atom, hydroxy or acyloxy group, R16 represents a hydroxy or acyloxy group, and the chiral central carbon marked with a symbol * in said formula (11) alternatively has one of an R-configuration and an S-configuration, is disclosed. Further, intermediate products of the compound of the formula (11) are also disclosed. Still further, a process for manufacturing the above compounds is disclosed. The compound of the formula (11) is easily synthesized from an easily available optically active starting material.

Enantio-and Stereo-controlled Construction of Tertiary and Quaternary Carbon Centers Using Chiral O-Benzylglycidol as Template

Takano, Seiichi,Shimazaki, Youichi,Moriya, Minoru,Ogasawara, Kunio

, p. 1177 - 1180 (2007/10/02)

An efficient method for the enantio- and stereo-controlled construction of tertiary and quaternary carbon centers in a highly functionalized system has been developed using chiral O-benzylglycidol as template.

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