Cas 1201638-76-7,(2R,3R,4S,5R,6R)-2-allyl-5-[(4-methoxybenzyl)oxy]-4,6-dimethylheptane-1,3,7-triol

1201638-76-7

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Basic information

Product Name: (2R,3R,4S,5R,6R)-2-allyl-5-[(4-methoxybenzyl)oxy]-4,6-dimethylheptane-1,3,7-triol
Synonyms: (2R,3R,4S,5R,6R)-2-allyl-5-[(4-methoxybenzyl)oxy]-4,6-dimethylheptane-1,3,7-triol
CAS NO:1201638-76-7
Molecular Formula:
Molecular Weight: 352.471
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: (2R,3R,4S,5R,6R)-2-allyl-5-[(4-methoxybenzyl)oxy]-4,6-dimethylheptane-1,3,7-triol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S,5R,6R)-2-allyl-5-[(4-methoxybenzyl)oxy]-4,6-dimethylheptane-1,3,7-triol(1201638-76-7)
EPA Substance Registry System: (2R,3R,4S,5R,6R)-2-allyl-5-[(4-methoxybenzyl)oxy]-4,6-dimethylheptane-1,3,7-triol(1201638-76-7)

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: 1201638-76-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201638-76-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,3 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1201638-76:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*3)+(3*8)+(2*7)+(1*6)=117
117 % 10 = 7
So 1201638-76-7 is a valid CAS Registry Number.

1201638-76-7Upstream product

1201638-76-7Downstream Products

1201638-78-9 (2R,3R,4R)-4-[(4R,5R)-5-allyl-2,2-dimethyl-1,3-dioxan-4-yl]-3-[(4-methoxybenzyl)oxy]-2-methylpentan-1-ol

1201638-76-7Relevant academic research and scientific papers

Total synthesis of the marine polypropionates, siphonarienal, siphonarienone, and pectinatone

Sabitha, Gowravaram,Gopal, Peddabuddi,Yadav, Jhillu S.

experimental part, p. 2205 - 2210 (2010/03/24)

The synthesis of the marine natural products, siphonarienal, siphonarienone, and pectinatone is described employing desymmetrization strategy to create three consecutive stereogenic centers. The key intermediate 7 was made by asymmetric hydroboration of t

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