Cas 201422-11-9,(1S,5S,7S)-7-benzyloxy-8,8-dimethyl-2,9-dioxabicyclo[3.3.1]nonan-3-one

201422-11-9

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Basic information

Product Name: (1S,5S,7S)-7-benzyloxy-8,8-dimethyl-2,9-dioxabicyclo[3.3.1]nonan-3-one
Synonyms: (1S,5S,7S)-7-benzyloxy-8,8-dimethyl-2,9-dioxabicyclo[3.3.1]nonan-3-one
CAS NO:201422-11-9
Molecular Formula:
Molecular Weight: 276.332
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: (1S,5S,7S)-7-benzyloxy-8,8-dimethyl-2,9-dioxabicyclo[3.3.1]nonan-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,5S,7S)-7-benzyloxy-8,8-dimethyl-2,9-dioxabicyclo[3.3.1]nonan-3-one(201422-11-9)
EPA Substance Registry System: (1S,5S,7S)-7-benzyloxy-8,8-dimethyl-2,9-dioxabicyclo[3.3.1]nonan-3-one(201422-11-9)

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: 201422-11-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201422-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,2 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 201422-11:
(8*2)+(7*0)+(6*1)+(5*4)+(4*2)+(3*2)+(2*1)+(1*1)=59
59 % 10 = 9
So 201422-11-9 is a valid CAS Registry Number.

201422-11-9Upstream product

21932-54-7 diisopinocampheylborane

201422-11-9Downstream Products

201422-11-9Relevant academic research and scientific papers

Synthesis of the C1-C9 segment of bryostatin

Weiss, Jochen M.,Hoffmann

, p. 3913 - 3920 (1997)

The C1-C9 segment of bryostatin has been prepared in 11 steps in 21% overall yield.

Asymmetric synthesis of the northern half C1-C16 of the bryostatins

Vakalopoulos,Lampe,Hoffmann

, p. 929 - 932 (2007/10/03)

matrix presented Starting from 8-oxabicyclo[3.2.1]oct-6-en-3-one and racemic 2,2-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one, the C1-C16 segment of the bryostatins has been synthesized in 30 steps and 9% overall yield (17 steps longest linear sequence). Fr

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