Cas 76101-86-5,n-butyl (<1R*,2S*,4S*>-2-<(1E)-6-((tert-butyldimethylsilyl)oxy)-1-heptenyl>-4-hydroxycyclopentyl)acetate

76101-86-5

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Basic information

Product Name: n-butyl (<1R^*,2S^*,4S^*>-2-<(1E)-6-((tert-butyldimethylsilyl)oxy)-1-heptenyl>-4-hydroxycyclopentyl)acetate
Synonyms: n-butyl (<1R^*,2S^*,4S^*>-2-<(1E)-6-((tert-butyldimethylsilyl)oxy)-1-heptenyl>-4-hydroxycyclopentyl)acetate
CAS NO:76101-86-5
Molecular Formula:
Molecular Weight: 426.712
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: n-butyl (<1R^*,2S^*,4S^*>-2-<(1E)-6-((tert-butyldimethylsilyl)oxy)-1-heptenyl>-4-hydroxycyclopentyl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: n-butyl (<1R^*,2S^*,4S^*>-2-<(1E)-6-((tert-butyldimethylsilyl)oxy)-1-heptenyl>-4-hydroxycyclopentyl)acetate(76101-86-5)
EPA Substance Registry System: n-butyl (<1R^*,2S^*,4S^*>-2-<(1E)-6-((tert-butyldimethylsilyl)oxy)-1-heptenyl>-4-hydroxycyclopentyl)acetate(76101-86-5)

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: 76101-86-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76101-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,0 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76101-86:
(7*7)+(6*6)+(5*1)+(4*0)+(3*1)+(2*8)+(1*6)=115
115 % 10 = 5
So 76101-86-5 is a valid CAS Registry Number.

76101-86-5Upstream product

694-98-4 norborn-5-en-2-one

76101-86-5Downstream Products

76101-86-5Relevant academic research and scientific papers

Efficient Stereocontrolled Total Syntheses of Racemic and Natural Brefeldin-A

Drian, Claude Le,Greene, Andrew E.

, p. 5473 - 5483 (1982)

Brefeldin-A, an antiobiotic fungal metabolite, has been obtained in both racemic and natural forms through a direct approach that employs norbornenone and 6-heptyn-2-ol as the basic starting materials.

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