Cat. No JK807555_100_MG
J&K Chemical

Product Information

Product Name
(S)-2-(1R,2R)-2-3,5-Bis(tert-butyl)-2-hydroxyphenylmethyleneaminocyclohexylthioureido-N-benzyl-N,3,3-trimethylbutanamide, 95%
Brand Name
J&K
Product Number
807555
CAS
479423-24-0
Molecular Formula
C36H54N4O2S
Molecular Weight
606.90
SDS Document
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
135423393
IUPAC Name
(2S)-N-benzyl-2-(1R,2R)-2-(3,5-ditert-butyl-2-hydroxyphenyl)methylideneaminocyclohexylcarbamothioylamino-N,3,3-trimethylbutanamide
InChI Key
IJFFARBIZKKZOA-QPWMFTQFSA-N
SMILES
CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)O)C=NC@@H2CCCCC@H2NC(=S)NC@H(C(=O)N(C)CC3=CC=CC=C3)C(C)(C)C

Properties

Melting Point
118-128
Optical Activity
-104 to -94 (C=1, CHCl3, 22℃)

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Mannich Reaction of Ketene Silyl Acetals with Imines

Publication Name: Science of Synthesis
Publication Date: 2012

Use of Chiral Thioureas

Publication Name: Science of Synthesis
Publication Date: 2011

Recent Advances in Stereoselective Syntheses Using N-Acylimines

Publication Name: Synthesis
Publication Date: 2007-01
DOI: 10.1055/s-2006-958957

Thiourea Derivative Catalyzed Asymmetric Aza-Baylis–Hillman Reaction

Publication Name: Synfacts
Publication Date: 2005-12-16
DOI: 10.1055/s-2005-921710

(S)-2-[[(1R,2R)-2-[[[3,5-Bis(tert-butyl)-2-hydroxyphenyl]methylene]amino]cyclohexyl]thioureido]-N-benzyl-N,3,3-trimethylbutanamide, 95%

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