Weight | 183.254 g/mol |
---|---|
Formula | C13H13N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Aminodiphenylmethane (91-00-9)
benzhydrylamine
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- Preparation and use of benzhydrylamine polymers in peptide synthesis. II. Syntheses of thyrotropin releasing hormone, thyrocalcitonin 26-32, and eledoisin. (Journal of Organic Chemistry, 1974)
- Comparative use of benzhydrylamine and chloromethylated resins in solid-phase synthesis of carboxamide terminal peptides. Synthesis of oxytocin derivatives (Journal of Organic Chemistry, 1977)
- A gradative deprotection strategy for the solid-phase synthesis of peptide amides using p-(acyloxy)benzhydrylamine resin and the SN2 deprotection method (Journal of Organic Chemistry, 1985)
- Study of benzhydrylamine-type polymers. Synthesis and use of p-methoxybenzhydrylamine resin in the solid-phase preparation of peptides (Journal of Organic Chemistry, 1976)
- Luteinizing hormone releasing factor. The total solid-phase synthesis on a benzhydrylamine polymer (Biochemical and Biophysical Research Communications, 1972)
- Kinetics of Synthesis and Swelling Studies of Highly Substituted Benzhydrylamine-Resins: Implications for Peptide Synthesis and Perspectives for Use as Anion Exchanger Resin (Journal of the Brazilian Chemical Society, 1992)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzhydrylamine
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SMILESC1=CC=C(C=C1)C(C2=CC=CC=C2)N
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InChIKeyMGHPNCMVUAKAIE-UHFFFAOYSA-N
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