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2-(4-Methylphenoxy)benzenamine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100712-95-6

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100712-95-6 Usage

Molecular weight

233.71 g/mol This is the mass of one mole of 2-(4-Methylphenoxy)benzenamine hydrochloride, based on the atomic weights of the elements that make up the compound.

Appearance

White to off-white crystalline solid This describes the physical appearance of the compound, which can be important for its identification and handling.

Solubility

Soluble in water and ethanol, slightly soluble in diethyl ether This indicates the solubility of the compound in different solvents, which can be important for its use in chemical reactions and pharmaceutical formulations.

Stability

Stable under normal conditions This indicates that the compound is not prone to decomposition or reaction under typical storage and handling conditions.

Reactivity

May react with strong acids, bases, or oxidizing agents This indicates the potential reactivity of the compound with other chemicals, which can be important for its handling and use in chemical reactions.

Uses

Synthesis of pharmaceuticals and organic intermediates This describes the common uses of the compound, which can be important for its production and distribution.

Handling and disposal

Handle with caution and dispose of properly to minimize health and environmental hazards This indicates the potential hazards associated with the compound and the need for proper handling and disposal practices.

Check Digit Verification of cas no

The CAS Registry Mumber 100712-95-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,1 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100712-95:
(8*1)+(7*0)+(6*0)+(5*7)+(4*1)+(3*2)+(2*9)+(1*5)=76
76 % 10 = 6
So 100712-95-6 is a valid CAS Registry Number.

100712-95-6Downstream Products

100712-95-6Relevant academic research and scientific papers

SYNTHESIS OF NITRODIBENZYLFURAN CHROMOPHORE FOR PHOTODEPROTECTION OF ORGANIC MOLECULES

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Page/Page column 26, (2008/06/13)

Inventors have developed a chromophore (nitrodibenzylfuranyl, or NBDF) for ultra efficient uncaging of a caged substrate (e.g., an organic molecule such as, for example, an amino acid, a biological molecules, such as, for example, second messengers inside cells). Photolysis of a NBDF derivative of EGTA (i.e. caged calcium) is about 50 times more efficient than others calcium cages (the quantum yield of photolysis is 0.6 and the extinction coefficient is 18,400. NDBF-EGTA has a 2-photon cross section of about 0.3-0.6 GM).

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