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N-benzylidene-N-cyclohexylamine oxide, also known as BCAO, is an organic compound with the chemical formula C13H17NO. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is often used as a chiral auxiliary in asymmetric synthesis. BCAO is a colorless, crystalline solid that is soluble in organic solvents. It is prepared by the reaction of cyclohexylamine with benzaldehyde in the presence of a base, such as sodium hydroxide. The compound is known for its ability to induce chirality in the molecules it interacts with, making it a valuable tool in the synthesis of enantiomerically pure compounds. BCAO is also used in the preparation of various pharmaceuticals and agrochemicals due to its ability to control the stereochemistry of reactions.

3376-25-8

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3376-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3376-25-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3376-25:
(6*3)+(5*3)+(4*7)+(3*6)+(2*2)+(1*5)=88
88 % 10 = 8
So 3376-25-8 is a valid CAS Registry Number.

3376-25-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexyl-1-phenylmethanimine oxide

1.2 Other means of identification

Product number -
Other names BENZYLIDENE-CYCLOHEXYL-OXIDO-AZANIUM

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3376-25-8 SDS

3376-25-8Relevant academic research and scientific papers

REGULATORS FOR CONTROLLING LINEAR AND PSEUDO-RING EXPANSION POLYMERIZATION OF VINYL MONOMERS

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Page/Page column 30; 35, (2017/07/01)

The invention concerns new regulator compounds for a novel polymerization process for vinyl monomers, which yields polymers with improved control over composition and nearly full to full conservation of architectural integrity up to high conversion. The regulator compounds are defined by according to anyone of the Formulas (1A), (1B), (1C), (1D), (1E), (1F), (1G), (1H) and (1I), wherein R1 stands for an optionally substituted secondary or tertiary alkyl or secondary or tertiary aralkyl; Z1 stands for -CN or a carboxylic acid ester of formula C(O)OR21; Z2 may be chosen from the group of -CN, carboxylic acid, salts of carboxylic acids, carboxylic acid ester, carboxylic acid amides, (hetero)aryl, alkenyl and halogen; R2, R3, R4 and R5 are each independently chosen from the group of H, alkyl, aralkyl, (hetero)aryl, -CN and carboxylic acid ester of formula C(O)OR22; R7 stands for a primary alkyl or primary aralkyl, -CN or hydrogen; Y stands for a bridging group and n is 2, 3, 4, 5 or 6; in case R1 stands for tertiary alkyl or tertiary aralkyl, R6 stands for a primary alkyl or primary aralkyl, -CN or a carboxylic acid ester of formula C(O)OR26; in case R1 stands for a secondary alkyl or secondary aralkyl, R6 stands for a primary or secondary alkyl or primary or secondary aralkyl, -CN, a carboxylic acid ester of formula C(O)OR26 or a phosphonic acid ester of formula P(O)(OR27)2, a (hetero)aryl or an alkenyl; R21, R22, R26 and R27 each independently stand for alkyl or aralkyi having from 1-30 carbon atoms, optionally containing heteroatoms.

Organotin-oxotungstate coordination polymer: An efficient catalyst for the selective oxidation of amines

Nikbakht, Fatemeh,Heydari, Akbar

, p. 132 - 136 (2015/03/04)

The organometallic coordination polymer [(nBu3Sn)2WO4] catalyzed the selective oxidation of secondary and primary amines to nitrones and oximes, respectively. The catalyst was found to be reusable for five catalytic cycles without any appreciable loss in activity. Under the optimized reaction conditions [4 mol% catalyst, 3-4 equiv of hydrogen peroxide (30 wt%, aqueous solution), methanol as the solvent, r.t.], the corresponding nitrones and oximes were obtained with good efficiency.

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