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88413-44-9

88413-44-9

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88413-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88413-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,1 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88413-44:
(7*8)+(6*8)+(5*4)+(4*1)+(3*3)+(2*4)+(1*4)=149
149 % 10 = 9
So 88413-44-9 is a valid CAS Registry Number.

88413-44-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1-thia-3-azaspiro[4.5]dec-2-ene

1.2 Other means of identification

Product number -
Other names -

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:88413-44-9 SDS

88413-44-9Downstream Products

88413-44-9Relevant articles and documents

STEREOCHEMICAL STUDIES, 66. SATURATED HETEROCYCLES, 51. SYNTHESIS OF STEREOISOMERIC 1,3-THIAZINES WITH CONDENSED SKELETON

Simon, Lajos,Talpas, Gizella S.,Fulop, Ferenc,Bernath, Gabor,Sohar, Pal

, p. 37 - 42 (2007/10/02)

cis- and trans-4,5-Tetramethylene-4,5-dihydro-6H-1,3-thiazines (2) were synthesized by heating the corresponding oxazines (1) with phosphorus pentasulfide.In the case of the 5,6-polymethylene analogues, trans-1,3-thiazines (4) were obtained from cis-1,3-o

Stereostructure of Condendsed-Skeleton cis- and trans-Dihydro-1,3-thiazines and 1-Thia-3-azaspiroalkenes

Sohar, P.,Simon, L.,Bernath, G.

, p. 597 - 602 (2007/10/02)

The stereostructures of some condensed-skeleton cis- and trans-dihydro-1,3-thiazines and 1-thia-2-phenyl-3-azaspiroalk-2-enes (n = 3-6) were established by 1H and 13C NMR spectroscopy.A comparative study indicated that the cis-thiazines have greater

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