6283-12-1 Usage
Nitroalkane derivative
It is a derivative of nitroalkanes A class of organic compounds containing a nitro group (-NO2) attached to an alkane carbon chain.
Dioxane ring
A six-membered cyclic ether structure The compound contains a 1,3-dioxane ring, which is a six-membered ring with two oxygen atoms connected by carbon atoms.
Methoxyphenyl group
Presence of a phenyl group with a methoxy substituent (-OCH3) A phenyl group (a benzene ring) is attached to the dioxane ring, and it has a methoxy group as a substituent, enhancing its reactivity and biological activity.
Organic synthesis and pharmaceutical research
Widely used in these fields The compound is commonly used in organic synthesis and pharmaceutical research due to its unique chemical properties.
Antimicrobial and antifungal activities
Potential applications in fighting infections The compound is known for its potential to exhibit antimicrobial and antifungal properties, making it a valuable compound in various scientific applications.
Reactivity and biological activity
Influenced by methyl and nitro groups The presence of a methyl group (-CH3) and a nitro group (-NO2) in the molecule contribute to its reactivity and biological activity, making it a valuable compound in scientific research and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6283-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6283-12:
(6*6)+(5*2)+(4*8)+(3*3)+(2*1)+(1*2)=91
91 % 10 = 1
So 6283-12-1 is a valid CAS Registry Number.
6283-12-1Relevant academic research and scientific papers
Catalytically Enantioselective Synthesis of Acyclic α-Tertiary Amines through Desymmetrization of 2-Substituted 2-Nitro-1,3-diols
Meng, Shan-Shui,Tang, Wu-Bang,Zheng, Wen-Hua
supporting information, p. 518 - 521 (2018/02/10)
Highly enantioselective synthesis of acyclic α-tertiary amines through asymmetric desymmetrization is reported. This approach is based on chiral phosphoric acid mediated, enantioselective, oxidative desymmetrization of 2-substituted 2-nitro-1,3-diolbenzylidine acetals in the presence of DMDO as an oxidant. The method allows for the formation of a wide variety of chiral 2-nitro-1,3-diols in high enantioselectivity, which could be transformed into optically pure, unnatural α-alkyl series. The synthetic utility of this method has been further demonstrated by the expedient construction of the core structure of natural products manzacidins enantioselectively.
Novel method of synthesizing unnatural chiral serine
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Paragraph 0033; 0034, (2017/08/29)
The invention belongs to the field of organic synthesis, in particular to a novel method of synthesizing unnatural chiral serine; according to the method, 2-nitro-1,3-diol is desymmetrized to obtain 2-nitro substituted optically-active 1,3-diol compound at high yield and high enantioselectivity, and the compound is simply chemically converted to obtain a series of optically-pure unnatural chiral serine. The materials in the method are simple and easily accessible and low in price; chemical reaction has high yield, a target compound can be acquired at high yield, and a finally synthesized compound is widely applicable and has high commercial value.
