Catalog No.:AA00066D

102-97-6 | Benzenemethanamine, N-(1-methylethyl)-

Name: Name:Benzenemethanamine, N-(1-methylethyl)-
Brand: AABLOCKS
SKU: AA00066D
Availability: InStock
Rating: 90 (10 reviews)

Pack Size

Purity

Availability

Price(USD)

Quantity

100g

98%

in stock

$38.00 $27.00

- +

Technical Information
Properties
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00066D

Chemical Name:

Benzenemethanamine, N-(1-methylethyl)-

CAS Number:

102-97-6

Molecular Formula:

C10H15N

Molecular Weight:

149.2328

MDL Number:

MFCD00008863

SMILES:

CC(NCc1ccccc1)C

NSC Number:

60295

Properties

BP:

200.0°C

Form:

Solid

MP:

143°C (estimate)

Refractive Index:

n20/D 1.502(lit.)

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

2.3

Downstream Synthesis Route

2461-42-9

102-97-6

2349-27-1

[1]Miyano,Sotaro;Lu,LindaD.-L.;Viti,StevenM.;Sharpless,K.Barry[JournalofOrganicChemistry,1985,vol.50,#22,p.4350-4360]

6852-56-8

102-97-6

[1]AngewandteChemie,1981,vol.93,p.477-479

[2]JournalofOrganicChemistry,2006,vol.71,p.5951-5958

[3]TetrahedronLetters,2013,vol.54,p.2619-2622

[4]ACSCatalysis,2013,vol.3,p.678-684

[5]ChemicalCommunications,2016,vol.52,p.4768-4771

4254-67-5

102-97-6

2-(Benzyl-isopropyl-amino)-1-(4-benzyloxy-phenyl)-ethanone

[1]JournalofMedicinalChemistry,1981,vol.24,p.315-322

102-97-6

6852-56-8

[1]ChemicalCommunications,2014,vol.50,p.3277-3280

[2]OrganicLetters,2009,vol.11,p.4568-4571

[3]Patent:JP2015/168667,2015,A.Locationinpatent:Paragraph0056-0060

[4]JournaloftheChemicalSociety.PerkintransactionsII,1992,p.1213-1217

[5]SyntheticCommunications,2005,vol.35,p.1989-1995

[6]JournalofOrganicChemistry,1995,vol.60,p.2072-2076

[7]AngewandteChemie-InternationalEdition,2011,vol.50,p.657-660

[8]AngewandteChemie-InternationalEdition,2012,vol.51,p.2654-2657

[9]Chemistry-AEuropeanJournal,2013,vol.19,p.5654-5664

[10]JournalofOrganicChemistry,2013,vol.78,p.5627-5637

[11]DaltonTransactions,2014,vol.43,p.11959-11972

[12]RSCAdvances,2016,vol.6,p.38553-38557

[13]RSCAdvances,2017,vol.7,p.48848-48852

[14]Chemistry-AEuropeanJournal,2018,vol.24,p.15089-15095

[15]Patent:CN108623494,2018,A.Locationinpatent:Paragraph0025-0026;0060-0064

[16]ChemicalScience,2019,vol.10,p.8455-8460

[17]JournalofMaterialsChemistryA,2019,vol.7,p.27074-27080

[18]AngewandteChemie-InternationalEdition,2020,vol.59,p.9088-9093 Angew.Chem.,2020,vol.132,p.9173-9178,6

[19]ChemCatChem,2020,vol.12,p.3523-3529

100-52-7

75-31-0

102-97-6

[1]TetrahedronLetters,2006,vol.47,p.3633-3636

[2]Synthesis,2011,p.490-496

[3]Patent:WO2020/23355,2020,A1.Locationinpatent:Page/Pagecolumn167-168

[4]JournalofOrganicChemistry,1981,vol.46,p.3571-3574

[5]Synthesis,2000,p.789-800

[6]PharmaceuticalChemistryJournal,2000,vol.34,p.371-373

[7]AngewandteChemie-InternationalEdition,2017,vol.56,p.7218-7222 Angew.Chem.,2017,vol.129,p.7324-7328,5

[8]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.1965-1968

[9]Chemistry-AEuropeanJournal,2017,vol.23,p.2217-2224

[10]Tetrahedron,2017,vol.73,p.4616-4626

[11]Patent:WO2017/212289,2017,A1.Locationinpatent:Page/Pagecolumn22

[12]AdvancedSynthesisandCatalysis,2018,vol.360,p.1066-1071

Literature

Title: Lewis acid-promoted three-component reactions of propargylic alcohols with 2-butynedioates and secondary amines.

Journal: The Journal of organic chemistry 20111104

Title: Monoclinic modification of N-benzyl-propan-2-aminium chloride.

Journal: Acta crystallographica. Section E, Structure reports online 20100501

Title: N-Benzyl-propan-2-aminium chloride.

Journal: Acta crystallographica. Section E, Structure reports online 20100301

Title: Bis(N-benzyl-N-isopropyl-dithio-carbamato-κS)di-n-butyl-tin(IV).

Journal: Acta crystallographica. Section E, Structure reports online 20090501

Title: Intramolecular and intermolecular N-H...C(5)H(5)(-) hydrogen bonding in magnesocene adducts of alkylamines. Implications for chemical vapor deposition using cyclopentadienyl source compounds.

Journal: Journal of the American Chemical Society 20020925

Title: Catalytically active polymers obtained by molecular imprinting and their application in chemical reaction engineering.

Journal: Biomolecular engineering 20010801

Quotation Request

Company Name:

Contact Person:

Email:

Quantity Required:

Country:

Additional Info:

SDS