90121-03-2 Usage
Description
(3Z,6Z)-1-broMonona-3,6-diene, also known as (3Z,6Z)-1-bromo-3,6-diene, is an organic compound with the molecular formula C8H12Br2. It is classified as a diene, which means it contains two double bonds between carbon atoms. The chemical structure of (3Z,6Z)-1-bromo-3,6-diene consists of a linear chain of eight carbon atoms, with two bromine atoms attached to the first and third carbon atoms, and two double bonds at the third and sixth carbon atoms. (3Z,6Z)-1-broMonona-3,6-diene is known for its reactivity and versatility in organic synthesis, making it a valuable tool for creating various chemical compounds.
Uses
Used in Organic Synthesis:
(3Z,6Z)-1-broMonona-3,6-diene is used as a versatile building block in the field of organic synthesis for the creation of various chemical compounds. Its unique structure and reactivity allow it to participate in a wide range of chemical reactions, making it a valuable resource for organic chemists.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3Z,6Z)-1-broMonona-3,6-diene can be used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its reactivity and structural properties make it suitable for the development of new medications and therapeutic agents.
Used in Chemical Research:
(3Z,6Z)-1-broMonona-3,6-diene is also utilized in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic pathways. Its unique structure and reactivity provide opportunities for researchers to gain insights into the behavior of similar compounds and develop innovative strategies for chemical synthesis.
Used in Material Science:
In the field of material science, (3Z,6Z)-1-broMonona-3,6-diene can be employed as a component in the development of novel materials with specific properties. Its structural characteristics and reactivity may contribute to the creation of advanced materials with applications in various industries, such as electronics, aerospace, and automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 90121-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,2 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90121-03:
(7*9)+(6*0)+(5*1)+(4*2)+(3*1)+(2*0)+(1*3)=82
82 % 10 = 2
So 90121-03-2 is a valid CAS Registry Number.
90121-03-2Relevant articles and documents
Convenient conversion of cis-homoallylic alcohols into corresponding bromides with Ph3PBr2
Sandri,Viala
, p. 2945 - 2948 (1992)
A mild and easy worked up procedure using the cheap reagent Ph3PBr2 allowed us to improve the conversion of sensitive alcohols (homoallylic and acetalized) into their corresponding bromides in high yields.
Direct preparation of (Z,Z)-1,4-dienic units with a new C6 homologating agent: Synthesis of α-linolenic acid
Sandri,Viala
, p. 271 - 275 (2007/10/02)
Syntheses of two C6 homologating agents 2a and 2f are described. These agents allow direct access to the (Z,Z)-1,4-diene unit 3, a moiety present in a wide number of natural compounds. Compound 2a is prepared in 40% overall yield by selective epoxidation of methoxycyclohexa-1,4-diene followed by oxidative ring cleavage and transatalization. Compound 2f is obtained in 90% yield by a one-step oxidative dimerization of phosphonium salt 1. A short synthetic application of these two new C6 homologating agents to the synthesis of α-linolenic acid is described.
Syntheses of the leukotrienes C5, D5, and E5
Spur,Crea,Peters,Konig
, p. 280 - 282 (2007/10/02)
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