N-(Diphenylmethyl)methylamine - CAS 14683-47-7
Catalog: |
BB010126 |
Product Name: |
N-(Diphenylmethyl)methylamine |
CAS: |
14683-47-7 |
Synonyms: |
N-methyl-1,1-diphenylmethanamine |
IUPAC Name: | N-methyl-1,1-diphenylmethanamine |
Description: | N-(Diphenylmethyl)methylamine (CAS# 14683-47-7) is used for amidation in study of mechanism of amido-thiourea catalyzed enantioselective imine hydrocynation. |
Molecular Weight: | 197.28 |
Molecular Formula: | C14H15N |
Canonical SMILES: | CNC(C1=CC=CC=C1)C2=CC=CC=C2 |
InChI: | InChI=1S/C14H15N/c1-15-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11,14-15H,1H3 |
InChI Key: | SHDMMLFAFLZUEV-UHFFFAOYSA-N |
Boiling Point: | 310.4 °C at 760 mmHg |
Melting Point: | 38-42 °C |
Purity: | 95 % |
Density: | 1.04 g/cm3 |
Appearance: | Colorless crystalline |
MDL: | MFCD00467853 |
LogP: | 3.38630 |
GHS Hazard Statement: | H314 (90.48%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
KR-102163568-B1 | Fatty acid antifungal peptide and antifungal composition comprising the same | 20200821 |
KR-20200102973-A | Fatty acid antifungal peptide and antifungal composition comprising the same | 20200821 |
WO-2021211786-A1 | Thyclotides | 20200417 |
WO-2021159300-A1 | Adhesive composition, laminate, and package | 20200212 |
CN-111040038-A | Ii-Key hybrid polypeptide and preparation method and application of tumor vaccine thereof | 20191225 |
PMID | Publication Date | Title | Journal |
21445346 | 20110322 | Inhibition of multidrug resistance by SV40 pseudovirion delivery of an antigene peptide nucleic acid (PNA) in cultured cells | PloS one |
20725626 | 20100613 | Synthesis and g-quadruplex-binding properties of defined acridine oligomers | Journal of nucleic acids |
17445276 | 20070420 | Structure of alpha-conotoxin BuIA: influences of disulfide connectivity on structural dynamics | BMC structural biology |
11558592 | 20010901 | Evaluation of the trifluoromethanosulfonic acid/trifluoroacetic acid/thioanisole cleavage procedure for application in solid-phase peptide synthesis | Chemical & pharmaceutical bulletin |
Complexity: | 148 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 197.120449483 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 197.120449483 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 12 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.9 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Nitrogen Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS