Cas 858662-10-9,methyl 5-[N-benzyl-N-[(1,1-dimethylethoxy)carbonyl]amino]-5-deoxy-α-D-allohexofuranuronate 1,2,3-triacetate

858662-10-9

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Basic information

Product Name: methyl 5-[N-benzyl-N-[(1,1-dimethylethoxy)carbonyl]amino]-5-deoxy-α-D-allohexofuranuronate 1,2,3-triacetate
Synonyms:
CAS NO:858662-10-9
Molecular Formula:
Molecular Weight: 523.537
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: methyl 5-[N-benzyl-N-[(1,1-dimethylethoxy)carbonyl]amino]-5-deoxy-α-D-allohexofuranuronate 1,2,3-triacetate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-[N-benzyl-N-[(1,1-dimethylethoxy)carbonyl]amino]-5-deoxy-α-D-allohexofuranuronate 1,2,3-triacetate(858662-10-9)
EPA Substance Registry System: methyl 5-[N-benzyl-N-[(1,1-dimethylethoxy)carbonyl]amino]-5-deoxy-α-D-allohexofuranuronate 1,2,3-triacetate(858662-10-9)

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: 858662-10-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 858662-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,6,6 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 858662-10:
(8*8)+(7*5)+(6*8)+(5*6)+(4*6)+(3*2)+(2*1)+(1*0)=209
209 % 10 = 9
So 858662-10-9 is a valid CAS Registry Number.

858662-10-9Upstream product

67-56-1 methanol

858662-10-9Downstream Products

858662-10-9Relevant academic research and scientific papers

A formal synthesis of thymine polyoxin C

Harding, Kenn E.,Southard, Jack M.

, p. 1845 - 1854 (2007/10/03)

A convergent stereoselective synthesis of thymine polyoxin C 1 has been conducted utilizing the benzylimine of D-glyceraldehyde acetonide 7 as a chiral controller and 2-trimethylsilyloxy furan 8 as a four-carbon synthon. In the presence of catalytic BF3·OEt2, 8 has been found to add to 7 with a moderately high level of stereoselectivity. Intermediate 4-(aminoalkyl)-2-butenolide 6 proved to be an ideal candidate for elaboration to 3.

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