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ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Ethyl 3-exo-aminobicyclo[2.2.1]hept-5-ene-2-exo-carboxylate hydrochloride

    Cas No: 104770-18-5

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  • ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE

    Cas No: 104770-18-5

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  • 104770-18-5 Structure
  • Basic information

    1. Product Name: ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE
    2. Synonyms: ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE;DIEXO-3-AMINO-BICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXYLIC ACID ETHYL ESTER HYDROCHLORIDE;Ethyl3-exo-aminobicyclo[2.2.1]hept-5-ene-2-exo-carboxylateHCl;Ethyl 3-exo-aminobicyclo[2.2.1]hept-5-ene-2-exo-carboxylate hydrochloride,99%;(1R,2R,3S,4S)-ethyl 3-aminobicyclo[2.2.1]hept-5-ene-2-carboxylate hydrochloride
    3. CAS NO:104770-18-5
    4. Molecular Formula: C10H15NO2*ClH
    5. Molecular Weight: 217.69
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104770-18-5.mol
  • Chemical Properties

    1. Melting Point: 129-132 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: White to light beige/Fine Crystalline Powder
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE(104770-18-5)
    11. EPA Substance Registry System: ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-CARBOXYLATE HYDROCHLORIDE(104770-18-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104770-18-5(Hazardous Substances Data)

104770-18-5 Usage

Chemical Properties

white to light beige fine crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 104770-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,7 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104770-18:
(8*1)+(7*0)+(6*4)+(5*7)+(4*7)+(3*0)+(2*1)+(1*8)=105
105 % 10 = 5
So 104770-18-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2.ClH/c1-2-13-10(12)8-6-3-4-7(5-6)9(8)11;/h3-4,6-9H,2,5,11H2,1H3;1H/t6-,7+,8+,9-;/m0./s1

104770-18-5SDS

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 Ethyl 3-exo-aminobicyclo[2.2.1]hept-5-ene-2-exo-carboxylate hydrochloride

1.2 Other means of identification

Product number -
Other names ETHYL 3-EXO-AMINOBICYCLO[2.2.1]HEPT-5-ENE-2-EXO-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:104770-18-5 SDS

104770-18-5Relevant articles and documents

Stereocontrolled one-step synthesis of difunctionalised cispentacin derivatives through ring-opening metathesis of norbornene β-amino acids

Kiss, Lornd,Kardos, Mrton,Forr, Eniko,Fül?p, Ferenc

, p. 1283 - 1289 (2015/03/04)

Through the ring-opening metathesis of norbornene or oxanorbornene β-amino acids with ethylene in the presence of certain Ru catalysts, a facile and convenient stereocontrolled one-step method was devised for the preparation of divinylated cispentacins an

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.

Stereochemical Studies, 106. - Saturated Heterocycles, 110. - Synthesis of Methylene-bridged Partially Saturated Quinazolones

Stajer, Geza,Szabo, Angela E.,Fueloep, Ferenc,Bernath, Gabor,Sohar, Pal

, p. 259 - 264 (2007/10/02)

With imidates, esters (5-8) of di-endo (1 and 2) and di-exo (3 and 4) norbornane- and norbornene-β-amino acids yield methylene-bridged tetrahydro- (18 and 20) and hexahydro-4-quinazolinones (17 and 19); the reaction of the corresponding carboxamides (9-12

Stereochemical Studies. Part 103. Saturated Heterocycles. Part 107. Preparation of 3-Mono and 2,3-Di-substituted Pyrimidin-4(3H)-ones in Retro-Diels-Alder Reactions. The Correct 1,2-Disubstituted Structure of the Compounds previously described as 2,3-Disu

Stajer, Geza,Szabo, Angela E.,Bernath, Gabor,Sohar, Pal

, p. 237 - 240 (2007/10/02)

The orthofomate cyclization of carboxamides (4) obtained from 3-exo-aminobicyclohept-5-ene-2-exo-carboxylic acid (1) yielded intermediate 8,9,10-trinorbornene-fused pyrimidinones (5) and hence 3-substituted pyrimidin-4(3H)-ones (6) through the spli

Stereochemical Studies. 81 . Saturated Heterocycles. 69 . Preparation of Methylene-bridged 3,1-Benzoxazines, 3,1-Benzoxazin-2-ones and 3,1-Benzoxazine-2-thiones

Stajer, Geza,Szabo, Angela E.,Fueloep, Ferenc,Bernath, Gabor,Sohar, Pal

, p. 1373 - 1376 (2007/10/02)

3-exo-Aminobicyclohept-5-ene-2-exo-carboxylic acid and ethyl 3-endo-aminobicycloheptane-2-endo-carboxylate (6) were reduced with lithium aluminum hydride to the corresponding bicyclic aminoalcohols 3 and 4.These and the saturated endo-endo a

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