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28250-14-8

28250-14-8

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28250-14-8 Usage

Chemical Properties

white to almost white granular powder

Check Digit Verification of cas no

The CAS Registry Mumber 28250-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,5 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28250-14:
(7*2)+(6*8)+(5*2)+(4*5)+(3*0)+(2*1)+(1*4)=98
98 % 10 = 8
So 28250-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h7-8H,2-6,10H2,1H3/p+1/t7-,8-/m1/s1

28250-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl Trans-2-Amino-1-Cyclohexanecarboxylate Hydrochloride, 98%

1.2 Other means of identification

Product number -
Other names ethyl cis-2-amino-1-cyclohexane carboxylate hydrochloride

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:28250-14-8 SDS

28250-14-8Relevant articles and documents

Selective mGAT2 (BGT-1) GABA uptake inhibitors: Design, synthesis, and pharmacological characterization

Vogensen, Stine B.,J?rgensen, Lars,Madsen, Karsten K.,Borkar, Nrupa,Wellendorph, Petrine,Skovgaard-Petersen, Jonas,Schousboe, Arne,White, H. Steve,Krogsgaard-Larsen, Povl,Clausen, Rasmus P.

supporting information, p. 2160 - 2164 (2013/05/08)

β-Amino acids sharing a lipophilic diaromatic side chain were synthesized and characterized pharmacologically on mouse GABA transporter subtypes mGAT1-4. The parent amino acids were also characterized. Compounds 13a, 13b, and 17b displayed more than 6-fold selectivity for mGAT2 over mGAT1. Compound 17b displayed anticonvulsive properties inferring a role of mGAT2 in epileptic disorders. These results provide new neuropharmacological tools and a strategy for designing subtype selective GABA transport inhibitors.

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