Cas 183888-70-2,4,8-Dioxa-3,9-disilaundecan-6-one, 2,2,10,10-tetramethyl-3,3,9,9-tetraphenyl-5-[(phenylmethoxy)methyl]-, (S)-

183888-70-2

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Basic information

Product Name: 4,8-Dioxa-3,9-disilaundecan-6-one, 2,2,10,10-tetramethyl-3,3,9,9-tetraphenyl-5-[(phenylmethoxy)methyl]-, (S)-
Synonyms:
CAS NO:183888-70-2
Molecular Formula: C43H50O4Si2
Molecular Weight: 687.039
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4,8-Dioxa-3,9-disilaundecan-6-one, 2,2,10,10-tetramethyl-3,3,9,9-tetraphenyl-5-[(phenylmethoxy)methyl]-, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: 4,8-Dioxa-3,9-disilaundecan-6-one, 2,2,10,10-tetramethyl-3,3,9,9-tetraphenyl-5-[(phenylmethoxy)methyl]-, (S)-(183888-70-2)
EPA Substance Registry System: 4,8-Dioxa-3,9-disilaundecan-6-one, 2,2,10,10-tetramethyl-3,3,9,9-tetraphenyl-5-[(phenylmethoxy)methyl]-, (S)-(183888-70-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 183888-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183888-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,8,8 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 183888-70:
(8*1)+(7*8)+(6*3)+(5*8)+(4*8)+(3*8)+(2*7)+(1*0)=192
192 % 10 = 2
So 183888-70-2 is a valid CAS Registry Number.

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183888-70-2Relevant academic research and scientific papers

Synthesis of protected enantiopure erythrulose derivatives

Marco, J. Alberto,Carda, Miguel,Gonzalez, Florenci,Rodriguez, Santiago,Murga, Juan

, p. 1801 - 1810 (2007/10/03)

D- and L-Erythrulose derivatives 2-6 bearing protective O-silyl and O-benzyl groups in various positions were synthesized in enantiopure form from L-ascorbic acid, D-isoascorbic acid, and D-glucose. VCH Verlagsgesellschaft mbH, 1996.

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