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2,4-Dimethoxybenzylamine - ≥98% , CAS No.20781-20-8

In stock
SKU
D123129
Grouped product items
Product Name Qty
[D123129-5g] 2,4-Dimethoxybenzylamine (5g)
Special Price €8.59 Regular Price €12.93
[D123129-25g] 2,4-Dimethoxybenzylamine (25g)
Special Price €12.93 Regular Price €19.87
[D123129-100g] 2,4-Dimethoxybenzylamine (100g)
Special Price €43.30 Regular Price €64.99
[D123129-500g] 2,4-Dimethoxybenzylamine (500g)
Special Price €151.77 Regular Price €228.13

2,4-Dimethoxybenzylamine can be preprepared by reduction (NaBH4 , BF3.OEt2, THF) of 2,4-dimethoxybenzonitrile

2,4-Dimethoxybenzylamine is an amine nucleophile used to investigate the 1,4- reactivity of 5-bromo-2-indene-1-one.It may be used in the following studies:
· As an ammonia equivalent in the concise synthesis of a series of 2,4,5-trisubstituted oxazoles, via a tandem Ugi/Robinson-Gabriel reaction sequence.
· Total synthesis of (-)-muraymycin (MRY) D2 and its epimer, the antibacterial nucleoside natural product.
· Two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction.
· Synthesis of N-hydroxythiourea.
· Synthesis of anti-HIV-1 agents

More Information

More Information
CAS20781-20-8
SynonymsBB 0217924 | SCHEMBL153750 | 4,5-DIMETHOXY-2-FLUOROBENZYLCHLORIDE | 2,4-dimethoxybenzyl amine | (2,4-Dimethoxyphenyl)methanamine # | DB02249 | 2,4-Dimethoxy benzylamine | STK500978 | Hexane, spectrophotometric grade, >=95% | 2,4-Dimethyloxybenzylamine | D
Specifications & Purity≥98%
StorageProtected from light,Room temperature,Argon charged
Shipped InNormal
Product Description

2,4-Dimethoxybenzylamine can be preprepared by reduction (NaBH4 , BF3.OEt2, THF) of 2,4-dimethoxybenzonitrile

2,4-Dimethoxybenzylamine is an amine nucleophile used to investigate the 1,4- reactivity of 5-bromo-2-indene-1-one.It may be used in the following studies:
· As an ammonia equivalent in the concise synthesis of a series of 2,4,5-trisubstituted oxazoles, via a tandem Ugi/Robinson-Gabriel reaction sequence.
· Total synthesis of (-)-muraymycin (MRY) D2 and its epimer, the antibacterial nucleoside natural product.
· Two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction.
· Synthesis of N-hydroxythiourea.
· Synthesis of anti-HIV-1 agents
Pubchem Sid528755478
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/528755478
SensitivityAir Sensitive;Light sensitive
Mdl NumberMFCD00052393
EC Number672-586-1
PubChem CID597250
Molecular FormulaC9H13NO2

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