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4H-1,3-Oxazine, 5,6-dihydro-5-iodo-4-phenyl-2-(trichloromethyl)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104808-54-0

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104808-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104808-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,0 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104808-54:
(8*1)+(7*0)+(6*4)+(5*8)+(4*0)+(3*8)+(2*5)+(1*4)=110
110 % 10 = 0
So 104808-54-0 is a valid CAS Registry Number.

104808-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-5-iodo-4-phenyl-2-(trichloromethyl)-4,5-dihydro-1,3-oxazine

1.2 Other means of identification

Product number -
Other names (4S,5S)-5-Iodo-4-phenyl-2-trichloromethyl-5,6-dihydro-4H-[1,3]oxazine

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:104808-54-0 SDS

104808-54-0Downstream Products

104808-54-0Relevant articles and documents

Factors Affecting the Regioselection of the Allylic Imidates Iodocyclization

Bongini, Alessandro,Cardillo, Giuliana,Orena, Mario,Sandri, Sergio,Tomasini, Claudia

, p. 4905 - 4910 (2007/10/02)

The regiochemistry of thr iodocyclization reaction of allylic imidates leading to 4,5-dihydro-1,3-oxazoles or to 4,5-dihydro-1,3-oxazines strongly depends on the configuration of the double bond: (E)-allylic imidatesafford preferentially 4,5-dihydro-1,3-oxazines through a 6-endo closure, whereas (Z)-allylic imidates afford preferentially 4,5-dihydro-1,3-oxazoles through a 5-exo closure.Furthermore a study on the effect of an oxygen atom vicinal to the double bond is reported.

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