N13054
4-Nitrobenzyl bromide
99%
Synonym(s):
α-Bromo-4-nitrotoluene
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About This Item
Linear Formula:
O2NC6H4CH2Br
CAS Number:
Molecular Weight:
216.03
Beilstein:
742796
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
mp
96-99 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc(CBr)cc1
InChI
1S/C7H6BrNO2/c8-5-6-1-3-7(4-2-6)9(10)11/h1-4H,5H2
InChI key
VOLRSQPSJGXRNJ-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
>212.0 °F
Flash Point(C)
> 100 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Allergic contact dermatitis from para-nitrobenzyl bromide.
R Thompson et al.
Contact dermatitis, 38(4), 232-232 (1998-06-20)
Qing-Yuan Chen et al.
Di 1 jun yi da xue xue bao = Academic journal of the first medical college of PLA, 23(3), 273-276 (2003-03-26)
To synthesize p, p'-divinylazobenzene (DVAB). Wittig reagent was initially synthesized using P-nitrobenzyl bromide and triphenylphosphine, followed by reaction with formaldehyde to produce p-nitro styrene, which was then deoxidized by Zn/NaOH for the final product of DVAB. Fourier transform infrared spectroscopy
S Giorgini et al.
Italian general review of dermatology, 15(2), 107-112 (1978-05-01)
A case of occupational contact dermatitis in a female chemical pharmaceutical laboratory researcher is described. The allergological investigation revealed a state of sensitization to three mono-nitrobenzenes with halogen substitutions in the nucleus or a side chain. Problems related to sensitization
Ihor Kulai et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(63), 16066-16077 (2017-08-31)
Eight alkyl triarylstannanecarbodithioates were synthesized starting from the corresponding triarylstannyl chlorides. They were fully characterized by IR and
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