Cas 1259928-75-0,(3R,7R,10S)-10-[(tert-butyldiphenyl)silyl]oxy-7-hydroxy-3-methyl-5-methyleneundec-1-ene

1259928-75-0

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Basic information

Product Name: (3R,7R,10S)-10-[(tert-butyldiphenyl)silyl]oxy-7-hydroxy-3-methyl-5-methyleneundec-1-ene
Synonyms: (3R,7R,10S)-10-[(tert-butyldiphenyl)silyl]oxy-7-hydroxy-3-methyl-5-methyleneundec-1-ene
CAS NO:1259928-75-0
Molecular Formula:
Molecular Weight: 450.737
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: (3R,7R,10S)-10-[(tert-butyldiphenyl)silyl]oxy-7-hydroxy-3-methyl-5-methyleneundec-1-ene(CAS DataBase Reference)
NIST Chemistry Reference: (3R,7R,10S)-10-[(tert-butyldiphenyl)silyl]oxy-7-hydroxy-3-methyl-5-methyleneundec-1-ene(1259928-75-0)
EPA Substance Registry System: (3R,7R,10S)-10-[(tert-butyldiphenyl)silyl]oxy-7-hydroxy-3-methyl-5-methyleneundec-1-ene(1259928-75-0)

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: 1259928-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1259928-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,9,2 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1259928-75:
(9*1)+(8*2)+(7*5)+(6*9)+(5*9)+(4*2)+(3*8)+(2*7)+(1*5)=210
210 % 10 = 0
So 1259928-75-0 is a valid CAS Registry Number.

1259928-75-0Upstream product

1259928-75-0Downstream Products

1259928-93-2 C₄₄H₆₆O₄Si

1259928-75-0Relevant academic research and scientific papers

A concise total synthesis of amphidinolide T2

Li, Huoming,Wu, Jinlong,Luo, Jialu,Dai, Wei-Min

supporting information; experimental part, p. 11530 - 11534 (2010/11/24)

RCM+AD=T2: In the presence of the C16-methylene group, regioselective ring-closing metathesis (RCM) formed the (12E)-endocyclic double bond, which underwent Os-catalyzed asymmetric dihydroxylation (AD) to give the desired 12,13-diol intermediate required

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