16714-07-1

• 

• Basic information

  1. Product Name: 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose
  2. Synonyms: 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose;1,2:3,4-Di-O-isopropyliden- 6-deoxy-6-thio-alpha-D-galactopyranose;1,2:3,4-Di-O-isopropylidene-6-thio-α-D-galactopyranose;1,2:3,4-di-O-isopropylidene-6-deoxy-6-thio-α-D-galactopyranose;((3AR,5S,5AR,8AS,8BR)-2,2,7,7-TETRAMETHYLTETRAHYDRO-3AH-BIS([1,3]DIOXOLO)[4,5-B:4,5-D]PYRAN-5-YL)METHANETHIOL;3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose
  3. CAS NO:16714-07-1
  4. Molecular Formula: C₁₂H₂₀O₅S
  5. Molecular Weight: 276.3492
  6. EINECS: N/A
  7. Product Categories: Carbohydrates
  8. Mol File: 16714-07-1.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 347.4±37.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.141±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 9.31±0.10(Predicted)
  10. CAS DataBase Reference: 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose(16714-07-1)
  12. EPA Substance Registry System: 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose(16714-07-1)

• 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: 16714-07-1(Hazardous Substances Data)

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• Lower Price 1,2-3,4-Di-O-Isopropylidene-6-Mercapto-6-Deoxy-Alpha-D-Galactopyranose on stock

  Cas No: 16714-07-1

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• 1 Kilogram

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• Siwei Development Group Ltd.
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• 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose

  Cas No: 16714-07-1

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• 1 Milligram

• 5

• Xiamen Jenny Chemical Technology Co., Ltd.
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• 1,2:3,4-Diisopropyliden-6-deoxy-6-thio-alpha-d-galactopyranose

  Cas No: 16714-07-1

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• ((3AR,5S,5aR,8aS,8bR)-2,2,7,7-tetramethyltetrahydro-3aH-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran-5-yl)methanethiol

  Cas No: 16714-07-1

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• 10 Milligram

• Amadis Chemical Co., Ltd.
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• 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose

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16714-07-1 Usage

General Description

1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose is a chemical compound with a complex molecular structure. It is a derivative of a-D-galactopyranose with thiol and isopropylidene groups attached to specific carbon atoms. 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose is often used in organic synthesis as a protecting group for the hydroxyl groups of sugars, allowing for selective reactions to occur without affecting the rest of the molecule. It is also commonly used in the preparation of various glycoside derivatives and as a building block in the synthesis of more complex carbohydrates. Overall, 1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose plays a crucial role in the development of new pharmaceuticals, materials, and other biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 16714-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16714-07:
(7*1)+(6*6)+(5*7)+(4*1)+(3*4)+(2*0)+(1*7)=101
101 % 10 = 1
So 16714-07-1 is a valid CAS Registry Number.

16714-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	1,2:3,4-Di-O-isopropylidene-6-thio-a-D-galactopyranose

1.2 Other means of identification

Product number	-
Other names	6-thio-1,2:3,4-di-O-iso-propylidene-D-galactopyranose

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:16714-07-1 SDS

16714-07-1Upstream product

• 4026-28-2 1,2:3,4-di-O-isopropylidene-6-iodo-D-galactopyranose 
• 3646-73-9 α-D-galactopyranose 
• 71001-09-7 1,2:3,4-di-O-isopropylidene-6-O-trifluoromethanesulfonyl-α-D-galactopyranose 
• 10257-28-0 D-Galactose 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 16714-06-0 6-S-acetyl-6-deoxy-1,2:3,4-di-O-isopropylidene-6-thio-α-D-galactopyranose 
• 4478-43-7 (1,2:3,4-di-O-isopropylidene-6-O-(p-toluensulfonate))-D-galactopiranose 

16714-07-1Downstream Products

• 1153940-53-4 1,2:3,4-di-O-isopropylidene-6-S-(2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl)-6-thio-α-D-galactopyranose 
• 1450629-16-9 C₄₆H₇₆O₉SSi₃ 
• 1450629-17-0 C₃₇H₅₂O₉SSi 
• 1333122-82-9 bis(1,2:3,4-di-O-isopropylidene-α-D-galactopyranosyl)-6,6′-disulfide 
• 1201897-32-6 1,2;3,4-di-O-isopropylidene-6-thio-(3',4',6'-tri-O-benzyl-2'-C-acetylmethyl-2'-deoxy-β-D-glucopyranosyl)-α-D-galactopyranoside 
• 1032633-96-7 1,2:3,4-di-O-isopropylidene-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-galactopyranose 

16714-07-1Relevant articles and documents

-

Stout et al.

, p. 1331,1332, 1334, 1335 (1975)

-

Synthesis and membranoprotective properties of new disulfides with monoterpene and carbohydrate fragments

Pestova,Izmestev,Shevchenko,Rubtsova,Kuchin

, p. 723 - 731 (2015/11/27)

A cooxidation of carbohydrate and terpene thiols gives mixtures of disulfides containing 51 - 90% of the unsymmetric product. Membranoprotective and antioxidant properties of obtained unsymmetric and symmetric disulfides were evaluated based on their ability to inhibit the H2O2-induced hemolysis of erythrocytes, as well as the accumulation of secondary products of the peroxy oxidation of lipids and the oxidation of hemoglobin.

Umpolung reactivity in the stereoselective synthesis of S-linked 2-deoxyglycosides

Baryal, Kedar N.,Zhu, Danyang,Li, Xiaohua,Zhu, Jianglong

supporting information, p. 8012 - 8016 (2013/08/23)

Take control! An unprecedented sulfenylation of stereochemically defined 2-deoxyglycosyl lithium species with asymmetric sugar-derived disulfide acceptors enabled the stereoselective synthesis of both α- and β-S-linked 2-deoxyoligosaccharides. Reductive lithiation of 2-deoxyglycosyl phenylsulfides at -78°C provides predominantly axial glycosyl lithium species, which upon warming isomerize to predominantly equatorial lithium species (see scheme). Copyright

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