13895-92-6

• 

• Basic information

  1. Product Name: RUTARETIN
  2. Synonyms: RUTARETIN;[S,(-)]-2,3-Dihydro-9-hydroxy-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one;2,3-Dihydro-9-hydroxy-2α-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one;(-)-Racemol
  3. CAS NO:13895-92-6
  4. Molecular Formula: C14H14O5
  5. Molecular Weight: 262.26
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13895-92-6.mol
  9. Article Data: 4

• 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: RUTARETIN(CAS DataBase Reference)
  10. NIST Chemistry Reference: RUTARETIN(13895-92-6)
  11. EPA Substance Registry System: RUTARETIN(13895-92-6)

• 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: 13895-92-6(Hazardous Substances Data)

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• SDS
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• Article

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• ≥97% high purity high quality custom manufacturing natural extract Rutaretin 13895-92-6

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13895-92-6 Usage

General Description

Rutaretin is a chemical compound that combines tretinoin and retinol, both of which are forms of vitamin A. Tretinoin is a derivative of vitamin A that is used to treat acne and reduce the appearance of fine lines and wrinkles. Retinol is also a form of vitamin A and is known for its ability to improve the texture and tone of the skin. The combination of these two compounds in Rutaretin makes it a powerful treatment for acne, as well as for improving the overall health and appearance of the skin. It works by promoting cell turnover and stimulating collagen production, which leads to smoother, firmer, and more radiant skin. Rutaretin is commonly used in skincare products and is known for its ability to improve the overall health and appearance of the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 13895-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13895-92:
(7*1)+(6*3)+(5*8)+(4*9)+(3*5)+(2*9)+(1*2)=136
136 % 10 = 6
So 13895-92-6 is a valid CAS Registry Number.

13895-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2S)-9-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one

1.2 Other means of identification

Product number	-
Other names	-

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:13895-92-6 SDS

13895-92-6Upstream product

• 486-35-1 daphnetin 
• 159979-64-3 (E)-3-[4-(3-Methyl-but-2-enyloxy)-2,2-diphenyl-benzo[1,3]dioxol-5-yl]-acrylic acid methyl ester 
• 159979-66-5 4-(3-Methyl-but-2-enyl)-2,2-diphenyl-[1,3]dioxolo[4,5-h]chromen-8-one 
• 159979-63-2 (E)-3-(4-Hydroxy-2,2-diphenyl-benzo[1,3]dioxol-5-yl)-acrylic acid methyl ester 
• 159979-62-1 2,2-Diphenyl-[1,3]dioxolo[4,5-h]chromen-8-one 
• 115235-61-5 (E)-3-(4-Hydroxy-3,5-dimethoxy-phenyl)-acrylic acid (2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[1-(9-hydroxy-7-oxo-2,3-dihydro-7H-furo[3,2-g]chromen-2-yl)-1-methyl-ethoxy]-tetrahydro-pyran-2-ylmethyl ester 

13895-92-6Downstream Products

13895-92-6Relevant articles and documents

COUMARIN SULPHATES OF SESELI LIBANOTIS

Lemmich, John,Shabana, Marawan

, p. 863 - 866 (1984)

Three new sulphate ester salts derived from known coumarin alcohols - one of them tertiary - have been obtained from roots of Seseli libanotis subsp. eu-libanotis.Their structures were established as (2'S)-rutaretin-1''-sulphate, (3'R)-lomatin-3'-sulphate and (3'R,4'R)-khellactone-3'-sulphate.They were together with their parent alcohols characterized by 13C NMR spectroscopy.It is the first report on coumarin sulphates in plants.Key Word Index - Seseli libanotis subsp. eu-libanotis; Umbelliferae; dihydrofurocoumarins; dihydropyranocoumarins; coumarin sulphates; sulphate ester salts; FDMS; 13C NMR.

Natural Product Chemistry. Part 181. Investigations on the Synthesis of Dihydropyrano- and Dihydrofurano-coumarins by Application of Catalytic Enantioselective cis-Dihydroxylation

Reisch, Johannes,Voerste, Arnd A. W.

, p. 3251 - 3256 (2007/10/02)

As part of a study on the applicability of catalytic enantioselective cis-dihydroxylation for the synthesis of dihydropyrano- and dihydrofurano-anellated coumarins new routes to (-)-cis-khellactone 1b, (-)-trans-khellactone 1c and rutaretin 4 have been developed.

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