Cyclobutylmethylamine

Cyclobutylmethylamine Suppliers list
Company Name: Capot Chemical Co.,Ltd.
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Email: sales@capot.com
Products Intro: Product Name:Cyclobutylmethylamine
CAS:4415-83-2
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:Cyclobutylmethylamine
CAS:4415-83-2
Purity:98% Package:1KG;1USD
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:Cyclobutylmethanamine
CAS:4415-83-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-20491
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:1-CYCLOBUTYLMETHANAMINE
CAS:4415-83-2
Purity:99% Package:1kg
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
Email: joe@yuhengpharm.com
Products Intro: Product Name:cyclobutylmethanamine
CAS:4415-83-2
Purity:0.97 Package:1KG;25KG

Cyclobutylmethylamine manufacturers

Cyclobutylmethylamine Basic information
Uses
Product Name:Cyclobutylmethylamine
Synonyms:Cyclobutylmethylamine;Aminomethylcyclobutane;1-Cyclobutylmethylamine;cyclobutylmethanamine hydrochloride;Cyclobutylmethylamine 95%;Cyclobutylmethylamine ISO 9001:2015 REACH;Cyclobutanemethanamine (9CI, ACI);cyclobutylMethanaMine
CAS:4415-83-2
MF:C5H11N
MW:85.15
EINECS:
Product Categories:
Mol File:4415-83-2.mol
Cyclobutylmethylamine Structure
Cyclobutylmethylamine Chemical Properties
Boiling point 90.6±8.0 °C(Predicted)
density 0.889±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka10.50±0.29(Predicted)
form liquid
color Colourless
Safety Information
HS Code 2922390090
MSDS Information
Cyclobutylmethylamine Usage And Synthesis
UsesIt is an intermediate in organic synthesis and pharmaceutical research and development, and can be used in laboratory organic synthesis and chemical and pharmaceutical research and development processes.
SynthesisBorane (1M solution in THF, 68 ml, 67.8 mmol) was added dropwise to a cooled (0C) solution of cyclobutanenitrile (5.0 g, 61.6 mmol) in THF (7 ml) under nitrogen. The mixture was warmed to room temperature and heated to reflux for 17 hours. The mixture was then cooled to 0C and quenched by addition of MeOH (81 ml). The mixture was warmed to room temperature and the solvent was removed. The substance was redissolved in MeOH (50 ml) and acidified with concentrated hydrochloric acid. HCl (50 ml) was added and then heated to reflux for 2 hours. The solvent was removed and the residue was ground with Et 2 O and a white powder (4.51 g) was filtered.
Cyclobutylmethylamine Preparation Products And Raw materials
Tag:Cyclobutylmethylamine(4415-83-2) Related Product Information
trimethylamine oxide SILIBININ-N-METHYLGLUCAMINE, 95% (HPLC) Meglumine Trimethylamine Cyclobutanemethanol Flunixin Meglumin Xorphanol BUTORPHANOL Cogazocine Butorphanol tartrate Sibutramine 5-CYCLOBUTYL-5-PHENYLHYDANTOIN Miboplatin Methylamine 4-[(FURAN-2-YLMETHYL)-CARBAMOYL]-1,2,2-TRIMETHYL-SPIRO[2.3]HEXANE-1-CARBOXYLIC ACID TRANS-CYCLOBUTANE-1,2-DICARBOXAMIDE NALBUPHINE HYDROCHLORIDE Cyclobutylmethylamine hydrochloride