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(-) -Anicyphos

(-) -Anicyphos is a chiral catalyst with the activity of promoting the selectivity of specific reactions. (-) -Anicyphos is often used to synthesize complex chiral molecules in organic synthesis and shows excellent catalytic performance. By adjusting the reaction conditions, (-) -Anicyphos can significantly improve the stereospecificity of the product, providing an effective strategy for compound development.

Product Specifications

CAS Number

98674-83-0

UNSPSC

12352005

Hazard Statement

H315-H319-H335

Target

Biochemical Assay Reagents; HBV

Type

Reference compound

Related Pathways

Anti-infection; Others

Applications

COVID-19-anti-virus

Assay Protocol

https://www.medchemexpress.com/minus-anicyphos.html

Smiles

CC1(C)COP(=O)(O)O[C@@H]1C2=CC=CC=C2OC

Molecular Formula

C12H17O5P

Molecular Weight

272.23

Precautions

P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

References & Citations

[1]Liquid chromatographic determination of d-and l-amino acids by derivatization with o-phthaldialdehyde and N-isobutyryl-l-cysteine applications with reference to the analysis of peptidic antibiotics, toxins, drugs and pharmaceutically used amino acids|[2]Automated enantioseparation of amino acids by derivatization with o-phthaldialdehyde and n-acylated cysteines|[3]Determination of the absolute configuration of selenomethionine from antarctic krill by RP-HPLC/ICP-MS using chiral derivatization agents|[4]Application of chiral derivatizing agents in the high-performance liquid chromatographic separation of amino acid enantiomers: a review|[5]Liquid chromatographic determination of D- and L-amino acids by derivatization with o-phthaldialdehyde and N-isobutyryl-L-cysteine

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Frequently Asked Questions

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