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90481-32-6

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90481-32-6 Usage

General Description

"(3S,4S)-Pyrrolidine-3,4-diol" is a specific stereochemical isomer of pyrrolidine-3,4-diol. Stereoisomers are compounds that have the same molecular formula and sequence of bonded atoms, but they differ in the three-dimensional orientation of their atoms in space. Pyrrolidine is a heterocyclic organic compound that contains a five-membered ring with nitrogen as heteroatoms. The "3,4-diol" part of the name signifies the presence of two hydroxyl groups attached to the third and fourth carbon respectively. The (3S,4S) designation refers to the specific spatial configuration of these groups, following the Cahn-Ingold-Prelog priority rules. (3S,4S)-Pyrrolidine-3,4-diol could potentially exhibit properties and activities varying from other isomers of pyrrolidine-3,4-diol, depending on the specific context and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 90481-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,8 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90481-32:
(7*9)+(6*0)+(5*4)+(4*8)+(3*1)+(2*3)+(1*2)=126
126 % 10 = 6
So 90481-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO2/c6-3-1-5-2-4(3)7/h3-7H,1-2H2/t3-,4-/m0/s1

90481-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-Pyrrolidine-3,4-diol

1.2 Other means of identification

Product number -
Other names (3S,4S)-3,4-Dihydroxypyrrolidine

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:90481-32-6 SDS

90481-32-6Relevant articles and documents

Fmoc-protected iminosugar modified asparagine derivatives as building blocks for glycomimetics-containing peptides

Nuti, Francesca,Paolini, Ilaria,Cardona, Francesca,Chelli, Mario,Lolli, Francesco,Brandi, Alberto,Goti, Andrea,Rovero, Paolo,Papini, Anna M.

, p. 3965 - 3973 (2007)

CSF114(Glc) is the first synthetic Multiple Sclerosis Antigenic Probe able to identify autoantibodies in a statistically significant number of Multiple Sclerosis patients. The β-turn conformation of this glucopeptide is fundamental for a correct presentat

Compound JK-03M having higher protein kinase G inhibitory activity or pharmaceutically acceptable salt thereof and preparation method thereof

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Paragraph 0093; 0118; 0130-0132, (2018/11/03)

The invention discloses a compound which has higher protein kinase G inhibitory activity and is shown in a formula I or pharmaceutically acceptable salt thereof and a preparation method thereof. The compound JK-03M having the higher protein kinase G inhibitory activity comprises a pharmaceutical composition of a new compound and application of the new compound in treatment of pain, in particular to chronic pain. The formula (1) is shown in the description.

Compounds with higher PKG (protein kinase G) inhibitory activity and preparation method of compounds

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Paragraph 0154; 0155; 0156; 0157; 0158; 0159, (2016/10/08)

The invention discloses compounds which have higher PKG (protein kinase G) inhibitory activity and are represented as a formula I, pharmaceutically acceptable salts, pharmaceutical composition containing the novel compounds, as well as an application of the novel compounds in treatment of pain, especially chronic pain. The invention further discloses a preparation method of the compounds and new intermediates. R1 and R2 are the same or different and are selected from a group comprising halogen (such as F or Cl), C1-C6 alkoxy, C1-C6 alkyl, C2-C6 alkenyl and C2-C6 alkynyl; R3 is a terminal group and is selected from a group comprising H, halogen, alkyl, naphthenic base, alkenyl, alkynyl, aryl and heteroaryl; n is the number of repetitive units and is an integer in a range from 1 to 15.

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