10395-46-7

• 

• Basic information

  1. Product Name: [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol
  2. Synonyms: [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol;(1S,6R)-3,7,7-Trimethylbicyclo[4.1.0]heptane-3α,4β-diol;(1α,6α)-3,7,7-Trimethylbicyclo[4.1.0]heptane-3α,4β-diol
  3. CAS NO:10395-46-7
  4. Molecular Formula: C₁₀H₁₈O₂
  5. Molecular Weight: 170.24872
  6. EINECS: 233-856-0
  7. Product Categories: N/A
  8. Mol File: 10395-46-7.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 272.8°Cat760mmHg
  3. Flash Point: 126.6°C
  4. Appearance: /
  5. Density: 1.091g/cm³
  6. Vapor Pressure: 0.000766mmHg at 25°C
  7. Refractive Index: 1.52
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol(CAS DataBase Reference)
  11. NIST Chemistry Reference: [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol(10395-46-7)
  12. EPA Substance Registry System: [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol(10395-46-7)

• 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: 10395-46-7(Hazardous Substances Data)

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• (1S,3S,4S,6R)-3,7,7-trimethylnorcarane-3,4-diol

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• (1S,3S,4S,6R)-3,7,7-trimethylnorcarane-3,4-diol

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• [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol

  Cas No: 10395-46-7

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10395-46-7 Usage

General Description

The chemical "[1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol" is a bicyclic compound that contains two fused cyclohexane rings. It has a molecular formula of C10H18O2 and a molecular weight of 170.25 g/mol. The compound is a diol, meaning it contains two hydroxyl (OH) functional groups. The stereochemistry of the molecule is specified with the 1S-(1alpha,3alpha,4beta,6alpha) prefix, indicating the configuration of the four stereocenters in the molecule. [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol may have potential applications in the field of organic and medicinal chemistry due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 10395-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10395-46:
(7*1)+(6*0)+(5*3)+(4*9)+(3*5)+(2*4)+(1*6)=87
87 % 10 = 7
So 10395-46-7 is a valid CAS Registry Number.

InChI:InChI=1/C10H18O2/c1-9(2)6-4-8(11)10(3,12)5-7(6)9/h6-8,11-12H,4-5H2,1-3H3

10395-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	3,7,7-Trimethylbicyclo[4.1.0]heptane-3,4-diol

1.2 Other means of identification

Product number	-
Other names	PSEUDOCARENE

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:10395-46-7 SDS

10395-46-7Upstream product

• 936-91-4 α-3,4-Epoxycarane 
• 936-91-4 (1S,3R,4S,6R)-3,4-epoxycarane 
• 13466-78-9 3-carene 
• 936-92-5 (1S,3R,4S,6R)-3,4-epoxy-3,7,7-trimethylbicyclo[4.1.0]heptane 
• 498-15-7 (+)-Δ³-carene 
• 22556-08-7 trans-3,4-caranediol 
• 10395-46-7 1S,3R,4S,6R-(+)-3β,4β-caranediol 
• 33116-78-8 (1S,3R)-(+)-3-hydroxy-4-isocaranyl tosylate 
• 4017-81-6 (1S,3S,6R)-(-)-4-Caren-3α-ol 
• 936-91-4 3-carene epoxide 

10395-46-7Downstream Products

• 36482-69-6 (1R,4S,6S)-4-hydroxy-4,7,7-trimethylbicyclo[4.1.0]heptan-3-one 
• 33116-78-8 (1S,3R)-(+)-3-hydroxy-4-isocaranyl tosylate 
• 936-92-5 (1S,3R,4S,6R)-3,4-epoxy-3,7,7-trimethylbicyclo[4.1.0]heptane 
• 58930-63-5 (3¹R,3³S)-3²,3²-dimethyl-3(1,3)cyclopropyla-5-oxohexanoic acid 
• 24348-06-9 (+)-3β-hydroxy-4-caranone 
• 22556-08-7 trans-3,4-caranediol 

10395-46-7Relevant articles and documents

-

Kropp,P.J.

, p. 4926 - 4934 (1966)

-

MECHANISM OF REARRANGEMENT WITH CYCLOPROPYL INVOLVEMENT IN ACETYLOSIS OF β-3,4-EPOXYCARANE

Arbuzov, B. A.,Isaeva, Z. G.,D'yakonova, R. R.

, p. 1949 - 1951 (1980)

-

Monoterpenediol insect repellents

-

, (2008/06/13)

An insect repellent comprising as an active ingredient a monoterpenediol compound having the formula, STR1 wherein R1, R2 and R3 have either one of the following definitions: (i) all of R1, R2 and R3 are hydrogen, (ii) R1 is hydrogen and R2 and R3, taken together, form a carbon-carbon single bond, or (iii) R2 is hydrogen, R1 and R3, taken together, form a carbon-carbon single bond, and the hydroxyl bonded to the carbon atom marked with an asterisk takes an α-configuration.

Transformations of 3-carene oxide at rhenium-containing catalysts

Manukov, E. N.,Bazhina, G. N.

, p. 106 - 110 (2007/10/02)

The transformations of 3-carene oxide at rhenium-containing catalysts were studied.The introduction of rhenium into the catalytic system significantly increases the reaction rate and leads to the formation of compounds not previously encountered in the products from the isomerization of 3-carene oxide, i.e., 3-carene, 3(10),4-caradiene, 3,3,6-trimethylcycloheptanone, and 3-caren-10-ol.

STEREOCHEMISTRY OF THE CARANE SYSTEM. OXIDATION PRODUCTS OF ISOMERIC 3,4-CARANEDIOLS OBTAINED FROM (+)-3-CARENE

Hendrich, Aleksandra,Piatkowski, Krzysztof

, p. 73 - 84 (2007/10/02)

Oxidation of four isomeric 3,4-caranediols has been carried out and reaction products have been investigated.It has been found that cis-diols rather form cyclic ketals than are oxidized under conditions of the Jones reaction.The key intermediate for syntheses of chrysanthemic acid, (-)-2-acetonyl-3,3-dimethylcyclopropaneacetic acid was obtained exclusively by oxidation of (-)-3β,4α-caranediol.

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