292389
2-Bromoheptane
technical grade
Synonym(s):
1-Methylhexyl bromide
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About This Item
Linear Formula:
CH3CH2CH2CH2CH2CHBrCH3
CAS Number:
Molecular Weight:
179.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-824-3
Beilstein/REAXYS Number:
1731556
MDL number:
grade
technical grade
Quality Level
refractive index
n20/D 1.447 (lit.)
bp
64-66 °C/21 mmHg (lit.)
density
1.142 g/mL at 25 °C (lit.)
functional group
alkyl halide, bromo
SMILES string
CCCCCC(C)Br
InChI
1S/C7H15Br/c1-3-4-5-6-7(2)8/h7H,3-6H2,1-2H3
InChI key
HLAUCEOFCOXKNF-UHFFFAOYSA-N
Application
2-Bromoheptane has been used in the preparation of:
- racemic alcohol, 2-methylheptanol
- glutathione (GSH) derivatives
- GSH analog that contains tetrazole isostere (Tet-sHep)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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J Boruwa et al.
Bioorganic & medicinal chemistry letters, 14(13), 3571-3574 (2004-06-05)
The absolute stereochemistry of the new antifungal and antibacterial antibiotic produced by Streptomyces sp.201 has been established by achieving the total synthesis of the product. A series of analogues have also been synthesized by changing the side chain and their
Danny Burg et al.
Bioorganic & medicinal chemistry letters, 12(12), 1579-1582 (2002-06-01)
Glutathione (GSH) conjugates inhibit enzymes that are involved in drug metabolism and drug resistance, but their cellular uptake is very low. To improve membrane-permeability, we synthesized a novel GSH-conjugate analogue with a tetrazole carboxylate isostere at the glycine position. Introduction
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 292389-25G | 04061837857263 |
| 292389-100G | 04061837857256 |