Lactandrate

Base Information

Chemical Name:Lactandrate
CAS No.:43000-65-3
Molecular Formula:C₃₁H₄₄Cl₂N₂O₃
Molecular Weight:563.608
Hs Code.:
UNII:41DCR34631
DSSTox Substance ID:DTXSID40195626
Nikkaji Number:J64.508G
Wikidata:Q27258433
ChEMBL ID:CHEMBL4173153
Mol file:43000-65-3.mol

Synonyms:3-hydroxy-13-amino-13,17-seco-5alpha--androstan-17-oic-13,17-lactam p-N,N-bis(2-chloroethyl)aminophenylacetate;3-hydroxy-13-amino-13,17-secoandrostan-17-oic-13,17-lactam-4-bis(2-chloroethyl)aminophenylacetate;4 (N,N-bis(2-chloroethyl)amino)phenylacetate 3-hydroxy-17-aza-D-homoandrostan-17-one;NSC 290205;NSC 290205, (3alpha,5alpha)-isomer;NSC 620482;NSC-290205;NSC-620482;NSC-71964

Suppliers and Price of Lactandrate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of Lactandrate

Chemical Property:

Vapor Pressure:6.21E-19mmHg at 25°C
Boiling Point:690.8°Cat760mmHg
Flash Point:371.6°C
Density:1.22g/cm³
XLogP3:6.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:9
Exact Mass:562.2728987
Heavy Atom Count:38
Complexity:843

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC(CC1CCC3C2CCC4(C3CCC(=O)N4)C)OC(=O)CC5=CC=C(C=C5)N(CCCl)CCCl
Isomeric SMILES:C[C@]12CC[C@@H](C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CCC(=O)N4)C)OC(=O)CC5=CC=C(C=C5)N(CCCl)CCCl

Technology Process of Lactandrate

There total 1 articles about Lactandrate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 44.0%