Cas 1092695-75-4,tert-butyl[(2S,3S)-2,3-dichloro-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]diphenylsilane

1092695-75-4

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Basic information

Product Name: tert-butyl[(2S,3S)-2,3-dichloro-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]diphenylsilane
Synonyms: tert-butyl[(2S,3S)-2,3-dichloro-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]diphenylsilane
CAS NO:1092695-75-4
Molecular Formula:
Molecular Weight: 467.508
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: tert-butyl[(2S,3S)-2,3-dichloro-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]diphenylsilane(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl[(2S,3S)-2,3-dichloro-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]diphenylsilane(1092695-75-4)
EPA Substance Registry System: tert-butyl[(2S,3S)-2,3-dichloro-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]diphenylsilane(1092695-75-4)

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: 1092695-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092695-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,6,9 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1092695-75:
(9*1)+(8*0)+(7*9)+(6*2)+(5*6)+(4*9)+(3*5)+(2*7)+(1*5)=184
184 % 10 = 4
So 1092695-75-4 is a valid CAS Registry Number.

1092695-75-4Upstream product

1092695-98-1 C₂₄H₃₂O₄Si

1092695-75-4Downstream Products

1092696-30-4 C₂₁H₂₈Cl₂O₃Si

1092695-75-4Relevant academic research and scientific papers

Enantiocontrolled synthesis of polychlorinated hydrocarbon motifs: A nucleophilic multiple chlorination process revisited

Yoshimitsu, Takehiko,Fukumoto, Naoya,Tanaka, Tetsuaki

supporting information; experimental part, p. 696 - 702 (2009/06/28)

Polychlorinated hydrocarbon motifs have been synthesized in enantiomerically pure forms by means of nucleophilic multiple chlorinations of chiral epoxides, which stereospecifically incorporate halogen atoms into oxygenated molecular scaffolds. The present

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