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487-99-0

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487-99-0 Usage

Description

(2S,3R)-2,3-Dihydroxy-2-isopropylbutanoic acid [(1R,7aR)-hexahydro-1H-pyrrolizin-1-yl]methyl ester is a complex organic compound consisting of two main components. The first component, (2S,3R)-2,3-Dihydroxy-2-isopropylbutanoic acid, is a dihydroxy acid featuring two hydroxyl groups and an isopropyl side chain. The second component, [(1R,7aR)-hexahydro-1H-pyrrolizin-1-yl]methyl ester, is an ester with a hexahydro-1H-pyrrolizin-1-yl group. (2S,3R)-2,3-Dihydroxy-2-isopropylbutanoic acid [(1R,7aR)-hexahydro-1H-pyrrolizin-1-yl]methyl ester's structural features, including hydroxyl groups and the ester linkage, suggest potential biological or pharmaceutical applications, making it a molecule of interest for various fields.

Uses

Used in Pharmaceutical Industry:
(2S,3R)-2,3-Dihydroxy-2-isopropylbutanoic acid [(1R,7aR)-hexahydro-1H-pyrrolizin-1-yl]methyl ester is used as a potential pharmaceutical agent for its ability to interact with biological molecules due to the presence of hydroxyl groups and the ester linkage. These features may allow the compound to be utilized in drug design and development, targeting specific biological pathways or mechanisms.
Used in Chemical Research:
In the field of chemical research, (2S,3R)-2,3-Dihydroxy-2-isopropylbutanoic acid [(1R,7aR)-hexahydro-1H-pyrrolizin-1-yl]methyl ester serves as a subject for studying the properties and reactions of complex organic molecules. Its unique structure provides opportunities for exploring new chemical reactions, synthesis methods, and potential applications in material science.
Used in Biochemical Applications:
(2S,3R)-2,3-Dihydroxy-2-isopropylbutanoic acid [(1R,7aR)-hexahydro-1H-pyrrolizin-1-yl]methyl ester is used as a biochemical tool for investigating its interactions with enzymes, receptors, or other biological targets. The presence of hydroxyl groups and the ester linkage may enable the compound to modulate biological processes or serve as a starting point for developing new bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 487-99-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 487-99:
(5*4)+(4*8)+(3*7)+(2*9)+(1*9)=100
100 % 10 = 0
So 487-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H27NO4/c1-10(2)15(19,11(3)17)14(18)20-9-12-6-8-16-7-4-5-13(12)16/h10-13,17,19H,4-9H2,1-3H3/t11-,12+,13-,15+/m1/s1

487-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name lindelofine

1.2 Other means of identification

Product number -
Other names Lindelofine

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:487-99-0 SDS

487-99-0Upstream product

487-99-0Downstream Products

487-99-0Relevant articles and documents

The total synthesis of some pyrrolyzidine alkaloids and their absolute configuration.

Kochetkov,Likhosherstov,Kulakov

, p. 2313 - 2323 (2007/10/04)

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