13206-31-0

• 

• Basic information

  1. Product Name: 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid
  2. Synonyms: 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid;5,5-Dimethyl-2-(1-methylethyl)-4-thiazolidinecarboxylic acid
  3. CAS NO:13206-31-0
  4. Molecular Formula: C₉H₁₇NO₂S
  5. Molecular Weight: 203.30178
  6. EINECS: 236-174-1
  7. Product Categories: N/A
  8. Mol File: 13206-31-0.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 334.7°Cat760mmHg
  3. Flash Point: 156.2°C
  4. Appearance: /
  5. Density: 1.087g/cm³
  6. Vapor Pressure: 2.39E-05mmHg at 25°C
  7. Refractive Index: 1.496
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid(13206-31-0)
  12. EPA Substance Registry System: 2-isopropyl-5,5-dimethylthiazolidine-4-carboxylic acid(13206-31-0)

• 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: 13206-31-0(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 4-Thiazolidinecarboxylicacid, 5,5-dimethyl-2-(1-methylethyl)-

  Cas No: 13206-31-0

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• 4-Thiazolidinecarboxylicacid, 5,5-dimethyl-2-(1-methylethyl)-

  Cas No: 13206-31-0

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• 4-Thiazolidinecarboxylicacid, 5,5-dimethyl-2-(1-methylethyl)-

  Cas No: 13206-31-0

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• 4-Thiazolidinecarboxylicacid, 5,5-dimethyl-2-(1-methylethyl)- cas 13206-31-0

  Cas No: 13206-31-0

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13206-31-0 Usage

Uses

5,5-Dimethyl-2-(1-Methylethyl)-4-Thiazolidinecarboxylic Acid is a penicillamine analogue which is useful in the treatment of arthritis kidney stones and metal poisoning.

Check Digit Verification of cas no

The CAS Registry Mumber 13206-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13206-31:
(7*1)+(6*3)+(5*2)+(4*0)+(3*6)+(2*3)+(1*1)=60
60 % 10 = 0
So 13206-31-0 is a valid CAS Registry Number.

InChI:InChI=1/C9H17NO2S/c1-5(2)7-10-6(8(11)12)9(3,4)13-7/h5-7,10H,1-4H3,(H,11,12)

13206-31-0SDS

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	5,5-dimethyl-2-propan-2-yl-1,3-thiazolidine-4-carboxylic acid

1.2 Other means of identification

Product number	-
Other names	2-isopropyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid

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:13206-31-0 SDS

13206-31-0Upstream product

• 13195-38-5 2-isopropyl-5,5-dimethyl-thiazolidine-4-carboxylic acid amide; hydrochloride 
• 22572-05-0 penicillamine hydrochloride 
• 78-84-2 isobutyraldehyde 

13206-31-0Downstream Products

13206-31-0Relevant articles and documents

On the Reactivity of Penicillamine and its Derivatives. Joint Reaction of Elementary Sulfur and Gaseous Ammonia with Ketones, 97

Asinger, Friedrich,Gluzek, Karl-Heinz

, p. 47 - 63 (2007/10/02)

DL-penicillamine-hydrochloride was condensed with various aldehydes (1 - 22) and ketones (23 - 28) to the corresponding 5,5-dimethyl-thiazolidine-4-carboxylic acid hydrochlorides and the free bases respectively.Their methylesters were obtained with diazomethane or methanol (29 - 35).Various 5,5-dimethyl-thiazolidine-4-carboxylic acids were formylated in position 3 (36 - 39).The reactivity of the carboxylic group was studied for 3-formyl-2,2,5,5-tetramethyl-thiazolidine-4-carboxylic acid.Substituted N-penicillaminamides were obtained for the first time (40 - 53).Also some S-alkylated penicillamines were prepared (54 - 60).By diazotation of 2,2,5,5-tetramethyl-thiazolidine-4-carbonamide or of penicillaminamide itself, 2-carbamyl-3,3-dimethyl-ethylene-sulfide was obatined. - Keywords: 3-Formyl-2,2,5,5-tetramethyl-thiazolidine-carboxylic acid amides; N-Formyl-5,5-dimethyl-thiazolidine-4-carboxylic acids; S-Alkylpenicillamines

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