Cas 1101185-56-1,dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate

1101185-56-1

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Basic information

Product Name: dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate
Synonyms: dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate
CAS NO:1101185-56-1
Molecular Formula:
Molecular Weight: 639.81
EINECS: N/A
Product Categories: N/A
Mol File: 1101185-56-1.mol
Article Data: 1

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: dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate(1101185-56-1)
EPA Substance Registry System: dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate(1101185-56-1)

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: 1101185-56-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1101185-56-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,1,1,8 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1101185-56:
(9*1)+(8*1)+(7*0)+(6*1)+(5*1)+(4*8)+(3*5)+(2*5)+(1*6)=91
91 % 10 = 1
So 1101185-56-1 is a valid CAS Registry Number.

1101185-56-1Upstream product

1101185-56-1Downstream Products

1101185-57-2 dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(1-oxohexadecylamino)nonadec-5-enylphosphonate

1101185-56-1Relevant articles and documents

Syntheses of sphingomyelin methylene, aza, and sulfur analogues by the versatile olefin cross-metathesis method

Yamamoto, Tetsuya,Hasegawa, Hiroko,Ishii, Sekimi,Kaji, Satoshi,Masuyama, Tatsuro,Harada, Syuji,Katsumura, Shigeo

experimental part, p. 11647 - 11660 (2009/04/05)

The syntheses of optically homogeneous sphingomyelin analogues, which possess CH2, NH, and S instead of the phosphate oxygen connecting the phosphocholine head group to the sphingosine backbone, were successfully achieved by employing the olefi

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