Bromonitromethane

Modify Date: 2024-01-02 09:02:14

Bromonitromethane Structure
Bromonitromethane structure
Common Name Bromonitromethane
CAS Number 563-70-2 Molecular Weight 139.93600
Density 2.07 Boiling Point 146-148 °C (750 mmHg)
Molecular Formula CH2BrNO2 Melting Point N/A
MSDS Chinese USA Flash Point 4°C
Symbol GHS03 GHS07
GHS03, GHS07
Signal Word Danger

 Use of Bromonitromethane


Bromonitromethane is a halonitromethane that can be used in production of various protected α-bromo nitroalkane donors for use in Umpolung Amide Synthesis (UmAS)[1][2].

 Names

Name Bromonitromethane
Synonym More Synonyms

 Chemical & Physical Properties

Density 2.07
Boiling Point 146-148 °C (750 mmHg)
Molecular Formula CH2BrNO2
Molecular Weight 139.93600
Flash Point 4°C
Exact Mass 138.92700
PSA 45.82000
LogP 1.13870
Index of Refraction 1.485-1.495

 Safety Information

Symbol GHS03 GHS07
GHS03, GHS07
Signal Word Danger
Hazard Statements H272-H315-H319-H335
Precautionary Statements P220-P261-P305 + P351 + P338
Personal Protective Equipment Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
Hazard Codes O: Oxidizing agent;Xn: Harmful;
Risk Phrases R8;R36/37/38
Safety Phrases S36/37/39-S26-S17-S36
RIDADR 3098
RTECS PA5360000
Packaging Group III
Hazard Class 5.1
HS Code 2904909090

 Synthetic Route

 Customs

HS Code 2904909090
Summary HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

 Articles3

More Articles
Silyl imine electrophiles in enantioselective catalysis: a Rosetta Stone for peptide homologation, enabling diverse N-protected aryl glycines from aldehydes in three steps.

Org. Lett. , (2014)

We report that N-(trimethylsilyl)imines serve in the Bis(AMidine)-catalyzed addition of bromonitromethane with a high degree of enantioselection. This allows for the production of a range of protected...

Stereoselective synthesis of highly functionalized nitrocyclopropanes through the organocatalyic Michael-addition-initiated cyclization of bromonitromethane and β,γ-unsaturated α-ketoesters.

Chem. Asian J. 8(11) , 2859-63, (2013)

A highly diastereo- and enantioselective cyclopropanation of β,γ-unsaturated α-ketoesters with bromonitromethane has been successfully developed through a domino Michael-addition/intramolecular-alkyla...

Synthesis of enantiopure 2-C-glycosyl-3-nitrochromenes.

J. Org. Chem. 78(24) , 12831-6, (2013)

A novel methodology has been developed to obtain enantiopure 2-C-glycosyl-3-nitrochromenes. First, (Z)-1-bromo-1-nitroalkenes were prepared from the corresponding sugar aldehydes through a sodium iodi...

 Synonyms

MFCD00007401
EINECS 209-258-0
bromo(nitro)methane
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