Cas 136289-19-5,Acetic acid (2S,3R,4S,5S)-1-(1-benzenesulfonyl-2-methyl-propyl)-2,3,4-tris-benzyloxy-5-methoxy-6-(4-methoxy-benzyloxy)-hexyl ester

136289-19-5

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Basic information

Product Name: Acetic acid (2S,3R,4S,5S)-1-(1-benzenesulfonyl-2-methyl-propyl)-2,3,4-tris-benzyloxy-5-methoxy-6-(4-methoxy-benzyloxy)-hexyl ester
Synonyms: Acetic acid (2S,3R,4S,5S)-1-(1-benzenesulfonyl-2-methyl-propyl)-2,3,4-tris-benzyloxy-5-methoxy-6-(4-methoxy-benzyloxy)-hexyl ester
CAS NO:136289-19-5
Molecular Formula:
Molecular Weight: 825.033
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: Acetic acid (2S,3R,4S,5S)-1-(1-benzenesulfonyl-2-methyl-propyl)-2,3,4-tris-benzyloxy-5-methoxy-6-(4-methoxy-benzyloxy)-hexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2S,3R,4S,5S)-1-(1-benzenesulfonyl-2-methyl-propyl)-2,3,4-tris-benzyloxy-5-methoxy-6-(4-methoxy-benzyloxy)-hexyl ester(136289-19-5)
EPA Substance Registry System: Acetic acid (2S,3R,4S,5S)-1-(1-benzenesulfonyl-2-methyl-propyl)-2,3,4-tris-benzyloxy-5-methoxy-6-(4-methoxy-benzyloxy)-hexyl ester(136289-19-5)

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: 136289-19-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136289-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136289-19:
(8*1)+(7*3)+(6*6)+(5*2)+(4*8)+(3*9)+(2*1)+(1*9)=145
145 % 10 = 5
So 136289-19-5 is a valid CAS Registry Number.

136289-19-5Upstream product

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136289-19-5Relevant academic research and scientific papers

AN ENANTIOSPECIFIC APPROACH TOWARDS THE C10 SIDE-CHAIN OF BENGAMIDES

Gurjar, M. K.,Srinivas, N. R.

, p. 3409 - 3412 (1991)

An enantiospecific approach to the highly hydroxylated C10 side-chain, common to all bengamides, starting from α-D-glucoheptonic γ-lactone, has been described.

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