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3,5-diacetoxy-2-acetoxymethyl-6-phenethyl-tetrahydro-pyran-4-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85505-09-5

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85505-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85505-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,0 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85505-09:
(7*8)+(6*5)+(5*5)+(4*0)+(3*5)+(2*0)+(1*9)=135
135 % 10 = 5
So 85505-09-5 is a valid CAS Registry Number.

85505-09-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenyl-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)ethan

1.2 Other means of identification

Product number -
Other names tetra-O-acetyl-1-phenyl-D-glycero-D-gulo-3,7-anhydro-1,2-dideoxy-octitol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85505-09-5 SDS

85505-09-5Downstream Products

85505-09-5Relevant academic research and scientific papers

Knoevenagel condensation between C-glycoside and active methylene compounds without catalysts

Gu, Xiaomin,Fang, Zhijie

, p. 683 - 686 (2016/11/18)

A Knoevenagel condensation reaction between a C-glycoside based aromatic aldehyde and cyclic active methylene compounds such as barbituric acid, thiobarbituric acid, 1,3-dimethylbarbituric acid, 5,5-dimethyl-1,3-cyclohexanedione, 2,2-dimethyl-1,3-dioxane-

Effective friedel-crafts acylations of O- and C-arylglycosides with triflic acid

Hashimoto, Makoto,Takahashi, Miho

body text, p. 227 - 231 (2009/09/06)

Triflic acid is well known not only as a Friedel-Crafts promoter, but also as a deglycosidation reagent. In this study, we promote effective Friedel-Crafts acylations for O- or C-arylglucosides without deglycosidation and check their inhibitory activities for β-glucosidase.

O-Glycosyl Imidates, 19. - Reactions of Glycosyl Trichloroacetimidates with Silylated C-Nucleophiles

Hoffmann, Michael G.,Schmidt, Richard R.

, p. 2403 - 2419 (2007/10/02)

Reaction of O-benzyl-protected α-glycopyranosyl trichloroacetimidates 1 and the xylo analogues 7 with silyl enol ethers or allyltrimethylsilane as C-nucleophiles yields with zink chloride as catalyst mainly or exclusively α-C-glycosides (5a-α to 5h-α, 8b,

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