Cas 1236041-35-2,(3aR,6R,7R,7aR)-6-((1R,2R)-2-acetoxy-1,3-bis(benzyloxy)-propyl)-5-acetyl-2,2-dimethylhexa hydro-[1,3]dioxolo[4,5-c]pyridin-7-yl acetate

1236041-35-2

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Basic information

Product Name: (3aR,6R,7R,7aR)-6-((1R,2R)-2-acetoxy-1,3-bis(benzyloxy)-propyl)-5-acetyl-2,2-dimethylhexa hydro-[1,3]dioxolo[4,5-c]pyridin-7-yl acetate
Synonyms:
CAS NO:1236041-35-2
Molecular Formula:
Molecular Weight: 569.652
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: (3aR,6R,7R,7aR)-6-((1R,2R)-2-acetoxy-1,3-bis(benzyloxy)-propyl)-5-acetyl-2,2-dimethylhexa hydro-[1,3]dioxolo[4,5-c]pyridin-7-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6R,7R,7aR)-6-((1R,2R)-2-acetoxy-1,3-bis(benzyloxy)-propyl)-5-acetyl-2,2-dimethylhexa hydro-[1,3]dioxolo[4,5-c]pyridin-7-yl acetate(1236041-35-2)
EPA Substance Registry System: (3aR,6R,7R,7aR)-6-((1R,2R)-2-acetoxy-1,3-bis(benzyloxy)-propyl)-5-acetyl-2,2-dimethylhexa hydro-[1,3]dioxolo[4,5-c]pyridin-7-yl acetate(1236041-35-2)

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: 1236041-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1236041-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,0,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1236041-35:
(9*1)+(8*2)+(7*3)+(6*6)+(5*0)+(4*4)+(3*1)+(2*3)+(1*5)=112
112 % 10 = 2
So 1236041-35-2 is a valid CAS Registry Number.

1236041-35-2Upstream product

77-76-9 2,2-dimethoxy-propane

1236041-35-2Downstream Products

1236041-35-2Relevant academic research and scientific papers

Synthesis of 1,4-dideoxy-1,4-iminoheptitol and 1,5-dideoxy-1,5-iminooctitols from d-xylose

Kumar, Amit,Alam, Mohammed Abrar,Rani, Shikha,Vankar, Yashwant D.

experimental part, p. 1142 - 1148 (2010/09/12)

The synthesis of iminosugars from inexpensive d-xylose in high yields has been developed. The key step in this synthesis involves Wittig olefination or chelation-controlled attack of Grignard reagents on lactol and ring-closing metathesis using first or s

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