3207-12-3 Usage
General Description
2-Amino-2-methyl-1-propanol hydrochloride, also known as AMPH, is a chemical compound that is commonly used as a solvent and as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used as a corrosion inhibitor, a pH regulator, and as an intermediate in the production of surfactants and detergents. AMPH hydrochloride is an organic compound with the molecular formula C4H12ClNO and a molecular weight of 137.6 g/mol. It is a white crystalline solid that is soluble in water and alcohols, and it is commonly used in the production of emulsifiers, lubricants, and corrosion inhibitors in various industries. AMPH hydrochloride is considered to be relatively safe for use in industrial and laboratory settings, but it should be handled with care and stored in a cool, dry place away from direct sunlight and heat sources.
Check Digit Verification of cas no
The CAS Registry Mumber 3207-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3207-12:
(6*3)+(5*2)+(4*0)+(3*7)+(2*1)+(1*2)=53
53 % 10 = 3
So 3207-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N5O7P.ClH/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20;/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20);1H/t4-,6-,7-,10-;/m1./s1
3207-12-3Relevant articles and documents
PROCESS FOR PRODUCING SUBSTITUTED AMINO ALCOHOLS
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Page/Page column 38; 39, (2020/06/01)
The present invention relates to a process for producing a compound of the formula (I) comprising at least the process step: a) reacting a compound of the formula (II) with hydrogen and water in the presence of at least one homogeneous transition metal catalyst TMC 1.
Radical-mediated intramolecular β-C(sp3)-H amidation of alkylimidates: Facile synthesis of 1,2-amino alcohols
Mou, Xue-Qing,Chen, Xiang-Yu,Chen, Gong,He, Gang
supporting information, p. 515 - 518 (2018/01/19)
A new radical-mediated intramolecular β-C(sp3)-H amidation reaction of O-alkyl trichloro- or arylimidates is reported. Various oxazolines were efficiently prepared from easily accessible alcohol starting materials. The trichloro-oxazoline products can be hydrolyzed under mild conditions to give valuable 1,2-amino alcohols. This amidation reaction exhibits a broad substrate scope and good functional group tolerance, and offers a powerful means for the C(sp3)-H functionalization of alcohols. Mechanistic studies suggest that a sequence of 1,5-HAT of an imidate radical, iodination and cyclization might be operative.
