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934660-64-7

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934660-64-7 Usage

General Description

(S)-benzyl 2-aminoethylcarbamate, also known as N-Benzyl-2-aminopropan-1-ol, is a chemical compound with the molecular formula C11H16N2O2. It is a derivative of carbamic acid and is commonly used as a pharmaceutical intermediate for the synthesis of various drugs and medications. (S)-benzyl 2-aMinopropylcarbaMate is a white to off-white crystalline powder that is soluble in organic solvents such as ethanol and dimethyl sulfoxide. It is utilized in the production of antihistamines, antidepressants, and muscle relaxants, and has potential applications in the treatment of cardiovascular diseases and neurological disorders. However, it is important to handle this chemical with caution as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 934660-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,6,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 934660-64:
(8*9)+(7*3)+(6*4)+(5*6)+(4*6)+(3*0)+(2*6)+(1*4)=187
187 % 10 = 7
So 934660-64-7 is a valid CAS Registry Number.

934660-64-7Downstream Products

934660-64-7Relevant articles and documents

β-PNA: Peptide nucleic acid (PNA) with a chiral center at the β-position of the PNA backbone

Sugiyama, Toru,Imamura, Yasutada,Demizu, Yosuke,Kurihara, Masaaki,Takano, Masashi,Kittaka, Atsushi

supporting information; experimental part, p. 7317 - 7320 (2012/02/04)

Peptide nucleic acid (PNA) monomers with a methyl group at the β-position have been synthesized. The modified monomers were incorporated into PNA oligomers using Fmoc chemistry for solid-phase synthesis. Thermal denaturation and circular dichroism (CD) studies have shown that PNA containing the S-form monomers was well suited to form a hybrid duplex with DNA, whose stability was comparable to that of unmodified PNA-DNA duplex, whereas PNA containing the R-form monomers was not.

POLYCYCLIC CARBAMOYLPYRIDONE DERIVATIVE HAVING HIV INTEGRASE INHIBITORY ACTIVITY

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Page/Page column 123, (2010/11/24)

The present invention is to provide a novel compound (I), having the anti-virus activity, particularly the HIV integrase inhibitory activity, and a drug containing the same, particularly an anti-HIV drug, as well as a process and an intermediate thereof. Compound (I) wherein Z1 is NR4; R1 is hydrogen or lower alkyl; X is a single bond, a hetero atom group selected from O, S, SO, SO2 and NH, or lower alkylene or lower alkenylene in which the hetero atom group may intervene; R2 is optionally substituted aryl; R3 is hydrogen, a halogen, hydroxy, optionally substituted lower alkyl etc; and R4 and Z2 part taken together forms a ring, to form a polycyclic compound, including e.g., a tricyclic or tetracyclic compound.

Selective synthesis of carbamate protected polyamines using alkyl phenyl carbonates

Pittelkow, Michael,Lewinsky, Rasmus,Christensen, Jorn Bolstad

, p. 2195 - 2202 (2007/10/03)

Utilising alkyl phenyl carbonates, an economical, practical and versatile method for selective Boc, Cbz and Alloc protection of polyamines has been developed. This method allows Boc, Cbz and Alloc protection of primary amines in the presence of secondary amines by reaction of the polyamines with the alkyl phenyl carbonates. Also, this method allows mono carbamate protection of simple symmetrical aliphatic α,ω-alkanediamines in high yields with respect to the diamine. Finally, the method allows selective carbamate protection of a primary amine located on a primary carbon in the presence of a primary amine located on a secondary or a tertiary carbon in excellent yields.

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