121748-11-6

• 

• Basic information

  1. Product Name: threo-1-C-Syringylglycerol
  2. Synonyms: threo-1-C-Syringylglycerol
  3. CAS NO:121748-11-6
  4. Molecular Formula: C₁₁H₁₆O₆
  5. Molecular Weight: 244.24
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 121748-11-6.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: threo-1-C-Syringylglycerol(CAS DataBase Reference)
  10. NIST Chemistry Reference: threo-1-C-Syringylglycerol(121748-11-6)
  11. EPA Substance Registry System: threo-1-C-Syringylglycerol(121748-11-6)

• 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: 121748-11-6(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

121748-11-6 Suppliers

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• THREO-1-C-SYRINGYLGLYCEROL

  Cas No: 121748-11-6

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• Dayang Chem (Hangzhou) Co.,Ltd.
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• 1,2,3-Propanetriol,1-(4-hydroxy-3,5-dimethoxyphenyl)-, (1R,2R)-rel-

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• Hangzhou J&H Chemical Co., Ltd.
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• Acmec threo-1-C-Syringylglycerol T31760 5mg

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• 1,2,3-Propanetriol,1-(4-hydroxy-3,5-dimethoxyphenyl)-, (1R,2R)-rel-

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• shanghai Tauto Biotech Co., Ltd
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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• threo-1-C-Syringylglycerol(121748-11-6)[121748-11-6]

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• Shaanxi Cuicheng Biomedical Technology Co., Ltd.
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121748-11-6 Usage

Uses

threo-1-C-Syringylglycerol is a chemical constituent from Kandelia candel with possible inhibitory effects on pro-inflammatory cytokines production in LPS-stimulated bone marrow-derived dendritic cells (BMDCs).

Check Digit Verification of cas no

The CAS Registry Mumber 121748-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,4 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121748-11:
(8*1)+(7*2)+(6*1)+(5*7)+(4*4)+(3*8)+(2*1)+(1*1)=106
106 % 10 = 6
So 121748-11-6 is a valid CAS Registry Number.

121748-11-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	(1S,2S)-1-(4-Hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol

1.2 Other means of identification

Product number	-
Other names	syringoylglycerol

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:121748-11-6 SDS

121748-11-6Upstream product

• 1370004-84-4 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)syringoylglycerol 
• 93722-54-4 α-Acetoxy-α-<3,5-dimethoxy-4-acetoxy-benzoyl>-essigsaeure-ethylester 
• 94003-00-6 ethyl 2-bromo-3-(4-acetoxy-3,5-dimethoxyphenyl)-3-oxopropionate 
• 92582-51-9 3,5-Dimethoxy-4-acetoxy-benzoylessigsaeure-aethylester 

121748-11-6Downstream Products

121748-11-6Relevant articles and documents

New CuCl2-induced glucoside esters and other constituents from Portucala oleracea

Wu, Bin,Yu, Liyan,Wu, Xiaodan,Chen, Jianbo

body text, p. 68 - 73 (2012/04/11)

Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl2. A new sugar ester (3) and two known compounds (4 and 5) were also isolated. Their structures were established by spectroscopic means. The antioxidative activities of stress metabolites and the related isolates were evaluated by DPPH assay. The results showed that new stress-driven adducts of monolignans and monoterpenes with a glucose bridge exhibited much stronger antioxidative activities than other compounds.

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