Skip to Content
Merck
CN
All Photos(2)

Documents

227846

Sigma-Aldrich

Methyl 4-nitrobutyrate

97%

Sign Into View Organizational & Contract Pricing
All Photos(2)
Synonym(s):
4-Nitrobutyric acid methyl ester
Linear Formula:
O2N(CH2)3CO2CH3
CAS Number:
13013-02-0
Molecular Weight:
147.13
Beilstein:
1766154
EC Number:
235-866-0
MDL number:
MFCD00007408
UNSPSC Code:
12352100
PubChem Substance ID:
24853657
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.438 (lit.)

bp

106-110 °C/9 mmHg (lit.)

density

1.149 g/mL at 25 °C (lit.)

SMILES string

COC(=O)CCC[N+]([O-])=O

InChI

1S/C5H9NO4/c1-10-5(7)3-2-4-6(8)9/h2-4H2,1H3

InChI key

UBSPKGKFFQKZJB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

The reaction of methyl 4-nitrobutyrate with aldehydes, following the enantioselective Henry addition, was studied.

Other Notes

Remainder methyl 4-nitrovalerate

WGK

WGK 3

Flash Point(F)

185.0 °F

Flash Point(C)

85 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Gonzalo Blay et al.
Organic letters, 12(13), 3058-3061 (2010-06-12)
A catalytic highly enantioselective Henry addition of methyl 4-nitrobutyrate to aldehydes using a Cu(II)-amino pyridine complex as catalyst is described. The products resulting from this reaction constitute a new, highly versatile family of chiral building blocks as a result of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service