Welcome to LookChem.com Sign In|Join Free
  • or
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate is a complex organic compound with a unique chemical structure. It belongs to the pyrrolizidine alkaloid class, which are naturally occurring compounds found in various plant families and have potential applications in the pharmaceutical and chemical industries.

6029-84-1

Post Buying Request

6029-84-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6029-84-1 Usage

Uses

1. Used in Pharmaceutical Applications:
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate is used as a pharmaceutical compound for its potential therapeutic properties. (7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-(1 -hydroxyethyl)-3-methyl-butanoate's unique structure and functional groups may allow it to interact with biological targets, making it a candidate for the development of new drugs.
2. Used in Chemical Synthesis:
In the chemical industry, (7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate can be used as a building block or intermediate in the synthesis of more complex molecules. Its unique functional groups and structural features make it a valuable component in the creation of novel chemical entities.
3. Used in Insect Defense Mechanisms:
As a pyrrolizidine alkaloid, (7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-butanoate may be utilized by certain insects as a defense mechanism. These insects can sequester the compound from their food sources and use it for their own protection against predators.
4. Used in Medicinal Herb Preparations:
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2-(1 -hydroxyethyl)-3-methyl-butanoate may also be found in some medicinal herb preparations, where its potential therapeutic properties can be harnessed for various medicinal purposes. The specific applications and benefits of the compound in these preparations would depend on the particular herb and the intended use.

References

Akramov, Kiyamitdinova, Yunusov., Uzbek. Khirn. Zh., No.6, 36 (1961)

Check Digit Verification of cas no

The CAS Registry Mumber 6029-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6029-84:
(6*6)+(5*0)+(4*2)+(3*9)+(2*8)+(1*4)=91
91 % 10 = 1
So 6029-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H25NO5/c1-9(2)15(20,10(3)17)14(19)21-8-11-4-6-16-7-5-12(18)13(11)16/h4,9-10,12-13,17-18,20H,5-8H2,1-3H3

6029-84-1Downstream Products

6029-84-1Relevant academic research and scientific papers

Ideamine N-Oxides: Pyrrolizidine Alkaloids Sequestered by the Danaine Butterfly, Idea leuconoe

Nishida, Ritsuo,Kim, Chul-Sa,Fukami, Hiroshi,Irie, Ryozo

, p. 1787 - 1792 (2007/10/02)

Two new pyrrolizidine alkaloids, ideamines A and B, together with other analogs (lycopsamine and parsonsine) were isolated in the N-oxide forms from adult bodies of the Apocynaceae-feeding danaine butterfly, Idea leuconoe.Ideamine A was characterized as a homolog of lycopsamine, in which the viridifloric acid moiety was replaced by a 2-ethyl-2,3-dihydroxybutanoic moiety.Likewise, ideamine B was identified as a nor-derivative of parsonsine, in which the trachelanthic acid moiety was replaced by a 2-ethyl-2,3-dihydroxybutanoic moiety diastereomeric to the necic acid from ideamine A.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6029-84-1