| Weight | 105.922 g/mol |
|---|---|
| Formula | CBrN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
CYANOGEN BROMIDE (506-68-3)
Score:
#230 in Biochemistry
,
#898 in Biology
,
#993 in Chemistry
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- A simplified method for cyanogen bromide activation of agarose for affinity chromatography (Analytical Biochemistry, 1974)
- [27] The cyanogen bromide reaction (Methods in Enzymology, 1967)
- Amino acid sequence studies of horseradish peroxidase. Amino and carboxyl termini, cyanogen bromide and tryptic fragments, the complete sequence, and some structural characteristics of horseradish peroxidase C. (FEBS Journal, 1979)
- The progeny of rabbit articular chondrocytes synthesize collagen types I and III and type I trimer, but not type II. Verifications by cyanogen bromide peptide analysis. (Biochemistry, 1977)
- Identification of three genetically distinct collagens by cyanogen bromide cleavage of insoluble human skin and cartilage collagen (Biochemical and Biophysical Research Communications, 1971)
- Preparation of cyanogen bromide-activated agarose gels (Journal of Chromatography A, 1973)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(#N)Br
-
InChIKeyATDGTVJJHBUTRL-UHFFFAOYSA-N
- Pubchem - CYANOGEN BROMIDE
- Wikipedia - cyanogen bromide
Cyanogen bromide is the inorganic compound with the formula (CN)Br or BrCN. It is a colorless solid that is widely used to modify biopolymers, fragment proteins and peptides (cuts the C-terminus of methionine), and synthesize other compounds. The compound is classified as a pseudohalogen.
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CYANOGEN BROMIDE
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