1004538-34-4 Usage
General Description
The chemical (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate hydrochloride is a crystalline solid with a molecular formula C11H21N2O2Cl. It is a derivative of the amino acid proline and is commonly used as an intermediate in the synthesis of pharmaceutical compounds. (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate hydrochloride is widely utilized in organic synthesis for the preparation of various bioactive molecules, particularly in the development of pharmaceuticals. The hydrochloride salt form of (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate enhances its solubility and stability, making it more suitable for use in research and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1004538-34-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,4,5,3 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1004538-34:
(9*1)+(8*0)+(7*0)+(6*4)+(5*5)+(4*3)+(3*8)+(2*3)+(1*4)=104
104 % 10 = 4
So 1004538-34-4 is a valid CAS Registry Number.
InChI:InChI=1S/C9H18N2O2.ClH/c1-9(2,3)13-8(12)11-5-4-7(10)6-11;/h7H,4-6,10H2,1-3H3;1H/t7-;/m1./s1
1004538-34-4Relevant articles and documents
METHOD FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-NITROGENATED COMPOUND
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Page/Page column 22, (2009/05/29)
Aiming at production of an optically active 3-amino nitrogen-containing compound which is useful as an intermediate in synthesis of medicines and pesticides, in particular, an optically active 1-protected-3-aminopyrrolidine derivative, from an inexpensive and readily available raw material by a process which is efficient and can be practiced industrially, an optically active 3-amino nitrogen-containing compound is produced by performing a reaction of an optically active 3-substituted nitrogen-containing compound with ammonia, methylamine, ethylamine or dimethylamine in the presence of water. In addition, a 1-protected-3-aminopyrrolidine derivative is produced by performing a reaction of an optically active 1-protected-3-(sulfonyloxy)pyrrolidine derivative with ammonia, methylamine, ethylamine, or dimethylamine in the presence of methanol, ethanol, n-propanol, or isopropanol under a pressure of less than 30 barr.