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CHEMBRDG-BB 4141581, also known as 2-(1-amino-1-oxopentane-2,5-diyl)propyl dihydrogen phosphate, is a chemical compound with a molecular formula of C6H16NO5P. It is a reagent used in the synthesis of organic compounds and has potential biological activity, making it a candidate for pharmaceutical development.

91012-98-5

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91012-98-5 Usage

Uses

Used in Chemical Synthesis:
CHEMBRDG-BB 4141581 is used as a reagent for the synthesis of organic compounds, enabling a variety of chemical reactions.
Used in Pharmaceutical Development:
As a compound with potential biological activity, CHEMBRDG-BB 4141581 is studied for its possible role in pharmaceutical development, although further research is needed to fully understand and utilize its properties.
Used in Chemistry and Biology Research:
As a dihydrogen phosphate derivative, CHEMBRDG-BB 4141581 has the potential to contribute to various fields in chemistry and biology, expanding the scope of scientific inquiry and application.

Check Digit Verification of cas no

The CAS Registry Mumber 91012-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,1 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91012-98:
(7*9)+(6*1)+(5*0)+(4*1)+(3*2)+(2*9)+(1*8)=105
105 % 10 = 5
So 91012-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-11-9(10(12)13)7-3-5-8(14-2)6-4-7/h3-6,9,11H,1-2H3,(H,12,13)

91012-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-2-(methylamino)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:91012-98-5 SDS

91012-98-5Relevant articles and documents

1, 3-thiazolium-5-thiolates mesoionic compounds: Semiempirical evaluation of their first static hyperpolarizabilities and synthesis of new examples

Lyra, Bruno F.,De Morais, Soraya A.,Rocha, Gerd B.,Miller, Joseph,Moura, Gustavo L.C.,Simas, Alfredo M.,Peppe, Clovis,De Athayde-Filhoa, Petro?nio F.

experimental part, p. 934 - 940 (2010/09/08)

Semiempirical AM1-TDHF calculations of the static first hyperpolarizabilities, β(0), of 1, 3-thiazolium-5-thiolate mesoionic derivatives were performed. Guided by these results, two new mesoionic compounds - 2-(4-nitrophenyl)-3-methyl-4-(methylphenyl)-1,

Influence of the aromatic substitutes in the thermal and kinetic behavior of mesoionic compounds of the 1,3-thiazole-5-tiolate system

de Morais, Soraya Alves,da Silva Morais, Crislene Rodrigues,Filho, Petr?nio Filgueiras de Athayde,Lira, Bruno Freitas,Souza, Marcos Antonio feitosa de

scheme or table, p. 598 - 602 (2010/08/21)

In this work, three mesoionic compounds of the 1,3-thiazole-5-tiolat system were studied, derived from amino acids of the glycerin through 1,3-dipolar cyclo-addition/reversion reaction. The mesoionic compounds were characterized as: MI-1 (mesoionic 2-(4-chlorophenyl)-3-methyl-4-phenyl-1,3-thiazole-5-tiolat); MI-2 (mesoionic 2-(4-chlorophenyl)-3-methyl-4-(4-isopropylphenyl)-1,3-thiazole-5-tiolat) and MI-3 (Mesoionic 2-(4-clorophenyl)-3-methyl-4-(methoxyphenyl)-1,3-thiazole-5-tiolate). These compounds were characterized by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), thermogravimetry (TG) and differential scanning calorimeter (DSC). Also, the kinetic study of the thermal decomposition by non-isothermal thermogravimetry has been realized, presenting, the kinetic and thermal behavior of these compounds. The results of the spectroscopic analysis confirmed the structure of the synthesized mesoionic compounds. The DSC curves of the mesoionic compounds MI-1, MI-2, and MI-3 indicated the fusion of two of them followed by a subsequent decomposition. The TG/DTG curves showed that the decomposition of the mesoionic compounds MI-1, MI-2 and MI-3 occurred in several steps.

Synthesis and Antineoplastic Activity of Bisoxy>methyl>-Substituted 3-Pyrrolines as Prodrugs of Tumor Inhibitory Pyrrole Bis(carbamates)

Anderson, Wayne K.,Milowsky, Arnold S.

, p. 2241 - 2249 (2007/10/02)

A series of bispyrrolines 2-4 were synthesized from either the appropriate α-silylated iminium salt, or an aziridine, or a 2H-azirine in a sequence involving 1,3-dipolar cycloaddition reactions.The antineoplastic activities of the pyrrolines were compared to the corresponding pyrroles.The C-2 gem-dimethyl-substituted pyrroline, 4, which cannot be converted to the pyrrole in vivo, was inactive.The activity of the 2-phenyl-substituted pyrrolines 3 was markedly dependent on the nature of the phenyl substituent, although the correspondingphenylpyrroles all showed comparable activity.The differences in the activities of the pyrrolines 3 may be due to the rate of metabolic conversion of the pyrroline to the pyrrole.Electron-withdrawing substituents on the phenyl ring appear to retard this process.

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