2-Thiophenemethylam...

2-Thiophenemethylamine
2-Thiophenemethylamine
2-Thiophenemethylamine

2-Thiophenemethylamine

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1 Kilogram

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  • Min.Order :1 Kilogram
  • Purity: 98%
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2-Thiophenemethylamine 27757-85-3 C5H7NS

Quick Details

  • Appearance:powder
  • Application:27757-85-3
  • PackAge:as requested
  • ProductionCapacity:300|Kilogram|Month
  • Storage:store in cool, dry place
  • Transportation:by sea or by air

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2-Thiophenemethylamine Basic information
Product Name: 2-Thiophenemethylamine
Synonyms: RARECHEM AL BW 0257;THIOPHENE-2-METHYLAMINE;TIMTEC-BB SBB004315;2-Thienylmethanamine;LABOTEST-BB LT00053452;C-THIOPHEN-2-YL-METHYLAMINE;AKOS BBS-00003607;2-THIOPHENEMETHYLAMINE
CAS: 27757-85-3
MF: C5H7NS
MW: 113.18
EINECS: 248-639-6
Product Categories: Thiophene&Benzothiophene;Electronic Chemicals;Thiophens;Building Blocks;C4 to C6;Chemical Synthesis;Heterocyclic Building Blocks;Thiophenes
Mol File: 27757-85-3.mol
2-Thiophenemethylamine Structure
 
2-Thiophenemethylamine Chemical Properties
Boiling point  95-99 °C28 mm Hg(lit.)
density  1.103 g/mL at 25 °C(lit.)
refractive index  n20/D 1.5670(lit.)
Fp  165 °F
form  liquid
Sensitive  Air Sensitive
BRN  106296
CAS DataBase Reference 27757-85-3(CAS DataBase Reference)
NIST Chemistry Reference 2-Thiophenemethanamine(27757-85-3)
EPA Substance Registry System 2-Thiophenemethanamine(27757-85-3)
 
Safety Information
Hazard Codes  C
Risk Statements  34
Safety Statements  26-27-36/37/39-45-25
RIDADR  UN 3267 8/PG 2
WGK Germany  3
Hazard Note  Corrosive
HazardClass  8
PackingGroup  III
MSDS Information
Provider Language
2-(Aminomethyl)thiophene English
SigmaAldrich English
ACROS English
ALFA English
 
2-Thiophenemethylamine Usage And Synthesis
Chemical Properties Clear yellow liquid
Usage Reactant involved in synthesis of:• ;Triazole-linked-thiopene conjugates for use as a biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein1• ;Serotonin 5-HT1A receptor antagonists which have neuroprotective affects against ischemic cell damage2• ;Imidazole- and piperonyl-containing thiadiazoles and pyrimidines for use as inducible oxide synthase dimerization inhibitors3• ;Optoelectronic segmented polyurethanes4Reactant involved in:• ;Studies of organocatalyzed asymmetric reductive amination of ketones5• ;Metal-free ae

 

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