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80613-04-3

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80613-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80613-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80613-04:
(7*8)+(6*0)+(5*6)+(4*1)+(3*3)+(2*0)+(1*4)=103
103 % 10 = 3
So 80613-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c1-11-7(10)8-4-2-3-6(9)5-8/h6,9H,2-5H2,1H3

80613-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-hydroxypiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names LBN 557-077

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:80613-04-3 SDS

80613-04-3Relevant articles and documents

NEW 5-AMINOLEVULINIC ACID PRODRUGS FOR USE IN PHOTODYNAMIC THERAPY AND PHOTODYNAMIC DIAGNOSIS

-

Page/Page column 21; 23, (2010/04/06)

There is provided a compound of Formula (I) or (II) and salts thereof wherein R1 is an imine or an alkylated imine, said imine or alkylated imine comprising a linear or branched alkyl group of length C1 to C5; R2 are each independently (a) an unsubstituted or substituted linear or branched alkyl group of chain length C1-7; (b) an aryl substituted alkyl group, wherein said aryl group is substituted, (c) an alkoxy substituted alkyl group, wherein said alkoxy group is substituted by a methoxy group or an alkoxy group substituted with an alkoxy group,; or (d) an H atom; wherein said substituents in (a) and (b) are selected from hydroxy, alkoxy, acyloxy, alkoxycarbonyloxy, amino, aryl, nitro, oxo and fluoro groups. R3 and R4 are linear or branched alkyl groups of length C1 to C6 constituting a ketal or a cyclic ketal. The compounds claimed may be used for the manufacture of a medicament.

GABA uptake inhibitors. Syntheses and structure-activity studies on GABA analogues containing diarylbutenyl and diarylmethoxyalkyl N-substituents

Falch,Krogsgaard-Larsen

, p. 69 - 77 (2007/10/02)

A number of analogues of GABA or β-alanine containing 4,4-diphenyl-3-butenyl (DPB), benzhydryl ethyl ether (BEE), or benzhydryl propyl ether N-substituents have been synthesized and tested as inhibitors of synaptosomal GABA uptake. Whereas the N-DPB and N

Syntheses of Some Aminopiperidinecarboxylic Acids Related to Nipecotic Acid

Jacobsen, Poul,Schaumburg, Kjeld,Larsen, Jens-Joergen,Krogsgaard-Larsen, Povl

, p. 289 - 294 (2011/02/21)

This paper describes the syntheses of (3RS,5SR)-5-hydroxypiperidine-3-carboxylic acid (8), (3RS,5SR)-5-aminoperidine-3-carboxylic acid (9), (RS)-3-hydroxypiperidine-3-carboxylic acid (13), (RS)-α-amino-3-pyridineacetic acid (18), and α-amino-3-piperidineacetic acid (19), compound 19 probably being a mixture of diastereomeric racemates.The compounds 8 and 9 were prepared from 5-aminonicotinic acid by catalytic hydrogenation.The relative stereochemistry of 9 was established by 270 MHz 1H NMR spectroscopy.The α-hydroxy acid 13 was prepared via cyanhydrin reaction of the 3-piperidone derivative 11.The α-amino acids 18 and 19 were prepared from 3-pyridineacetic acid by nitrosation and subsequent catalytic hydrogenation.

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