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â-D-Glucopyranoside,2-(4-hydroxy-3- methoxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97400-08-3 Structure
  • Basic information

    1. Product Name: â-D-Glucopyranoside,2-(4-hydroxy-3- methoxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)-
    2. Synonyms:
    3. CAS NO:97400-08-3
    4. Molecular Formula:
    5. Molecular Weight: 476.478
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97400-08-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: â-D-Glucopyranoside,2-(4-hydroxy-3- methoxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)- (CAS DataBase Reference)
    10. NIST Chemistry Reference: â-D-Glucopyranoside,2-(4-hydroxy-3- methoxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)- (97400-08-3)
    11. EPA Substance Registry System: â-D-Glucopyranoside,2-(4-hydroxy-3- methoxyphenyl)ethyl 3-O-(6-deoxy-R-L-mannopyranosyl)- (97400-08-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 97400-08-3(Hazardous Substances Data)

97400-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97400-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,0 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97400-08:
(7*9)+(6*7)+(5*4)+(4*0)+(3*0)+(2*0)+(1*8)=133
133 % 10 = 3
So 97400-08-3 is a valid CAS Registry Number.

97400-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cistanoside E

1.2 Other means of identification

Product number -
Other names (2S,3R,4R,5R,6S)-2-{(2R,3R,4S,5R,6R)-3,5-Dihydroxy-2-[2-(4-hydroxy-3-methoxy-phenyl)-ethoxy]-6-hydroxymethyl-tetrahydro-pyran-4-yloxy}-6-methyl-tetrahydro-pyran-3,4,5-triol

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:97400-08-3 SDS

97400-08-3Upstream product

97400-08-3Downstream Products

97400-08-3Relevant articles and documents

Synthesis of carbohydrate-based natural products from leonurus japonicus and their biological evaluation as anti-oxidants

Clayton, Evette,Hattie, Mitchell,Debowski, Aleksandra W.,Stubbs, Keith A.

, p. 1461 - 1470 (2014)

Natural products are important materials that have found a wide variety of uses, especially in medicine. Traditional Chinese medicine (TCM) has especially taken advantage of natural products and compounds found in Leonurus, a species of herb used extensiv

Collective syntheses of phenylethanoid glycosides by interrupted Pummerer reaction mediated glycosylations

Zhao, Yueqi,Zeng, Jing,Liu, Yan,Xiao, Xiong,Sun, Guangfei,Sun, Jiuchang,Shu, Penghua,Fu, Dengxian,Meng, Lingkui,Wan, Qian

, p. 471 - 497 (2019/04/10)

The collective total syntheses of nine natural phenylethanoid glycosides (PhEGs) together with proposed Incanoside B in a divergent mode were described. By using a core disaccharide as common intermediate, our developed interrupted Pummerer reaction media

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