163169-10-6 Usage
General Description
IP-FOXAP is a chemical compound used as a selective herbicide for controlling certain grasses and broadleaf weeds in various crops, including corn, soybeans, and wheat. It works by inhibiting the enzyme acetolactate synthase, which is essential for the production of branched-chain amino acids in plants. This leads to the disruption of plant growth and ultimately results in the death of the targeted weeds. IP-FOXAP is applied as a post-emergence treatment and has shown effectiveness against a range of problematic weed species, making it a valuable tool for weed management in agriculture. However, it is important to follow the product label instructions and safety precautions when using IP-FOXAP to minimize potential harm to non-target organisms and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 163169-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,1,6 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 163169-10:
(8*1)+(7*6)+(6*3)+(5*1)+(4*6)+(3*9)+(2*1)+(1*0)=126
126 % 10 = 6
So 163169-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C23H23NOP.C5H5.Fe/c1-17(2)21-16-25-23(24-21)20-14-9-15-22(20)26(18-10-5-3-6-11-18)19-12-7-4-8-13-19;1-2-4-5-3-1;/h3-15,17,21H,16H2,1-2H3;1-5H;/t21-;;/m1../s1/rC28H28FeNOP/c1-21(2)26-20-31-27(30-26)25-18-11-19-28(25,29-22-12-9-10-13-22)32(23-14-5-3-6-15-23)24-16-7-4-8-17-24/h3-19,21-22,26H,20H2,1-2H3/t26-,28?/m1/s1
163169-10-6Relevant articles and documents
Kinetic resolution of racemic ferrocenylphosphine compounds by enantioselective oxidation using cyclic selenoxides having a chiral ligand
Miyake, Yoshihiro,Yamauchi, Akiyoshi,Nishibayashi, Yoshiaki,Uemura, Sakae
, p. 381 - 387 (2007/10/03)
Cyclic selenoxides having an optically active binaphthyl skeleton work as the reagents for enantioselective oxidation of phosphines to the corresponding phosphine oxides. Treatment of a racemic 2-oxazolin-2-ylferrocenylphosphine with one of the selenoxides in carbon tetrachloride in the presence of phenol affords the corresponding phosphine oxide together with the unreacted starting phosphine, both with moderate enantioselectivities (the phosphine oxide, up to 13% ee; the phosphine, up to 29% ee).
