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(3R,4S)-3,4-Dimethyladipic acid dimethyl ester, also known as dimethyl (3R,4S)-3,4-dimethylhexanedioate, is a diester compound derived from (3R,4S)-3,4-dimethyladipic acid. It is a clear, colorless liquid with a slightly sweet odor and is soluble in most organic solvents. This chemical is commonly used as a building block in organic synthesis and serves as a solvent in various chemical reactions. Due to its potential harmful effects if ingested, inhaled, or comes into contact with the skin and eyes, it is important to handle this chemical with caution.

6076-81-9

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6076-81-9 Usage

Uses

Used in Organic Synthesis:
(3R,4S)-3,4-Dimethyladipic acid dimethyl ester is used as a building block in the synthesis of various organic compounds. Its versatile structure allows for the creation of a wide range of molecules, making it a valuable asset in the field of organic chemistry.
Used as a Solvent:
In the chemical industry, (3R,4S)-3,4-Dimethyladipic acid dimethyl ester is utilized as a solvent for different chemical reactions. Its solubility in most organic solvents makes it a suitable candidate for facilitating various chemical processes.
Used in Pharmaceutical Industry:
(3R,4S)-3,4-Dimethyladipic acid dimethyl ester may also find applications in the pharmaceutical industry, potentially serving as an intermediate in the development of new drugs or as a component in drug formulations.
Used in Research and Development:
Due to its unique properties and reactivity, (3R,4S)-3,4-Dimethyladipic acid dimethyl ester is employed in research and development settings to explore new chemical reactions, synthesize novel compounds, and study their properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6076-81-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6076-81:
(6*6)+(5*0)+(4*7)+(3*6)+(2*8)+(1*1)=99
99 % 10 = 9
So 6076-81-9 is a valid CAS Registry Number.

6076-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (3S,4R)-3,4-dimethylhexanedioate

1.2 Other means of identification

Product number -
Other names (3R,4S)-Dimethyl 3,4-dimethylhexanedioate

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:6076-81-9 SDS

6076-81-9Relevant academic research and scientific papers

Synthesis and in vivo evaluation of 3,4-disubstituted gababutins

Blakemore, David C.,Bryans, Justin S.,Carnell, Pauline,Field, Mark J.,Kinsella, Natasha,Kinsora, Jack K.,Meltzer, Leonard T.,Osborne, Simon A.,Thompson, Lisa R.,Williams, Sophie C.

scheme or table, p. 248 - 251 (2010/04/02)

A range of 3,4-alkylated five-membered ring derivatives of gabapentin were synthesised. One compound (21) had an excellent level of potency against α2δ and was profiled in in vivo models of pain and anxiety.

Stereoselective hydrocoupling of cinnamic acid esters by electroreduction: Application to asymmetric synthesis of hydrodimers

Kise, Naoki,Iitaka, Shumei,Iwasaki, Keisuke,Ueda, Nasuo

, p. 8305 - 8315 (2007/10/03)

The electroreduction of Ar-substituted methyl cinnamates in acetonitrile gave all-trans cyclized hydrodimers stereoselectively (58-90% de). In all cases, small amounts (2-symmetric dl-3,4-diaryladipic acids and trans-3,4-diarylcyclopentanones. The chiral auxiliary [(1R)-exo]-3-exo-(diphenylmethyl)borneol, prepared from (1R)-(+)-camphor, was highly effective for the stereoselective hydrocoupling of its cinnamates by electroreduction. From the resulting hydrodimers, (3R,4R)-3,4-diaryladipic acid esters and (3R,4R)-3,4-diarylhexane-1,6-diols were synthesized in 87-95% ee.

Synthetic Studies towards the Pinguisanes; Synthesis of 4-epi-Pinguisone

Baker, Raymond,Selwood, David L.,Swain, Christopher J.,Webster,Nigel M.H.,Hirshfield, Jordan

, p. 471 - 480 (2007/10/02)

Two procedures have been developed for the synthesis of the appropriate indene skeleton required for construction of pinguisone and 4-epi-pinguisone.Whereas 1-methoxy-3-(trimethylsiloxy)buta-1,3-diene (Danishefsky's diene) was completely unreactive toward

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