Cas 152035-85-3,1-[(4R,5R)-5-((1R,3R)-5-Benzyloxy-1,3-dimethoxy-pentyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethane-1,2-diol

152035-85-3

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Basic information

Product Name: 1-[(4R,5R)-5-((1R,3R)-5-Benzyloxy-1,3-dimethoxy-pentyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethane-1,2-diol
Synonyms: 1-[(4R,5R)-5-((1R,3R)-5-Benzyloxy-1,3-dimethoxy-pentyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethane-1,2-diol
CAS NO:152035-85-3
Molecular Formula:
Molecular Weight: 398.497
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: 1-[(4R,5R)-5-((1R,3R)-5-Benzyloxy-1,3-dimethoxy-pentyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethane-1,2-diol(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(4R,5R)-5-((1R,3R)-5-Benzyloxy-1,3-dimethoxy-pentyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethane-1,2-diol(152035-85-3)
EPA Substance Registry System: 1-[(4R,5R)-5-((1R,3R)-5-Benzyloxy-1,3-dimethoxy-pentyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethane-1,2-diol(152035-85-3)

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: 152035-85-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 152035-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,0,3 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 152035-85:
(8*1)+(7*5)+(6*2)+(5*0)+(4*3)+(3*5)+(2*8)+(1*5)=103
103 % 10 = 3
So 152035-85-3 is a valid CAS Registry Number.

152035-85-3Upstream product

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152035-85-3Relevant academic research and scientific papers

Synthesis of Acyclic Polyol Derivatives via Enzyme-Mediated Aldol Reaction

Matsumoto, Kazutsugu,Shimagaki, Masayuki,Nakata, Tadashi,Oishi, Takeshi

, p. 4935 - 4938 (2007/10/02)

Enzyme-mediated stereoselective aldol reaction between dihydroxyacetone phosphate (DHAP, 1) and (2R,4R)-6-benzyloxy-2,4-dimethoxyhexanal (8) was catalyzed by rabbit muscle aldolase (RAMA) to generate (3S,4R,5R,7R)-trihydroxyketone 12, which could be easily transformed to the masked polyhydroxylated compound 15 corresponding to the C-9-C-16 segment of pentamycin (6).

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