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Merck
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주요 문서

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107794

Sigma-Aldrich

2-Nitrobenzyl bromide

98%

동의어(들):

α-Bromo-2-nitrotoluene

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5 G
₩71,862
25 G
₩213,658

₩71,862

출고 가능일2025년 4월 25일세부사항

벌크 견적 요청
모든 사진(1)

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5 G
₩71,862
25 G
₩213,658

About This Item

Linear Formula:
O2NC6H4CH2Br
CAS Number:
3958-60-9
Molecular Weight:
216.03
Beilstein:
638991
EC Number:
223-558-9
MDL number:
MFCD00007184
UNSPSC 코드:
12352100
PubChem Substance ID:
24846780
NACRES:
NA.22

₩71,862

출고 가능일2025년 4월 25일세부사항

벌크 견적 요청

Quality Level

100

분석

98%

양식

solid

mp

44-46 °C (lit.)

작용기

bromo
nitro

SMILES string

[O-][N+](=O)c1ccccc1CBr

InChI

1S/C7H6BrNO2/c8-5-6-3-1-2-4-7(6)9(10)11/h1-4H,5H2

InChI key

HXBMIQJOSHZCFX-UHFFFAOYSA-N

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관련 카테고리

애플리케이션

2-Nitrobenzyl bromide was used for caging unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution[1]. It can be used in the synthesis of (R)- and (S)-3-amino-3,4-dihydro-1H-quinolin-2-one[2].

생화학적/생리학적 작용

2-Nitrobenzyl bromide reacts with L-cysteine to form S-2-nitrobenzyl-cysteine which was used for modification of ultra-low-gelling-temperature (ULGT) agarose[3].

픽토그램

Corrosion
GHS05

신호어

Danger

유해 및 위험 성명서

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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시험 성적서(COA)

Lot/Batch Number
STBL1463
STBK6371
STBK4666
STBJ8925
STBJ4110

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문서 라이브러리 방문

P Pan et al.
FEBS letters, 405(1), 81-85 (1997-03-17)
Photoreleasable molecules are important in studies of various biological phenomena, especially cell signaling. Here we report a generally applicable approach for 'caging' unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution with 2-nitrobenzyl bromides. Photolysis of the caged peptides was achieved
Ying Luo et al.
Nature materials, 3(4), 249-253 (2004-03-23)
Tissue engineering aims to replace, repair or regenerate tissue/organ function, by delivering signalling molecules and cells on a three-dimensional (3D) biomaterials scaffold that supports cell infiltration and tissue organization. To control cell behaviour and ultimately induce structural and functional tissue
Kyoung-Ho Park et al.
International journal of molecular sciences, 20(16) (2019-08-21)
A kinetic study was carried out on the solvolysis of o-nitrobenzyl bromide (o-isomer, 1) and p-nitrobenzyl bromide (p-isomer, 3), and o-nitrobenzoyl chloride (o-isomer, 2) in a wide range of solvents under various temperatures. In all of the solvents without aqueous
A practical synthesis of (R)-and (S)-3-amino-3, 4-dihydro-1H-quinolin-2-one.
Hulin B and Lopaze MG.
Tetrahedron Asymmetry, 15(12), 1957-1958 (2004)
Xu Yang et al.
Polymers, 12(4) (2020-04-09)
Photoresponsive polymers have attracted increasing interest for a variety of applications. Here, we report a family of photoresponsive polypeptoid-based copolymer poly(ethylene glycol)-b-poly(N-(S-(o-nitrobenzyl)-thioethyl) glycine)-co-poly(N-(2-phenylethyl) glycine) (PEG-b-PNSN-co-PNPE) synthesized by the controlled ring-opening polymerization (ROP) technique. The key feature of the design is
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