49751-88-4

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• Basic information

  1. Product Name: (1alpha,2alpha,5alpha)-6,6-dimethylbicyclo[3.1.1]heptane-2-carbaldehyde
  2. Synonyms: (1alpha,2alpha,5alpha)-6,6-dimethylbicyclo[3.1.1]heptane-2-carbaldehyde
  3. CAS NO:49751-88-4
  4. Molecular Formula: C₁₀H₁₆O
  5. Molecular Weight: 152.23344
  6. EINECS: 256-467-8
  7. Product Categories: N/A
  8. Mol File: 49751-88-4.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 200.7°Cat760mmHg
  3. Flash Point: 65.9°C
  4. Appearance: /
  5. Density: 1.013g/cm³
  6. Vapor Pressure: 0.32mmHg at 25°C
  7. Refractive Index: 1.528
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: (1alpha,2alpha,5alpha)-6,6-dimethylbicyclo[3.1.1]heptane-2-carbaldehyde(CAS DataBase Reference)
  11. NIST Chemistry Reference: (1alpha,2alpha,5alpha)-6,6-dimethylbicyclo[3.1.1]heptane-2-carbaldehyde(49751-88-4)
  12. EPA Substance Registry System: (1alpha,2alpha,5alpha)-6,6-dimethylbicyclo[3.1.1]heptane-2-carbaldehyde(49751-88-4)

• 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: 49751-88-4(Hazardous Substances Data)

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• (1alpha,2alpha,5alpha)-6,6-Dimethylbicyclo(3.1.1)heptane-2-carbaldehyde

  Cas No: 49751-88-4

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• (1alpha,2alpha,5alpha)-6,6-Dimethylbicyclo(3.1.1)heptane-2-carbaldehyde

  Cas No: 49751-88-4

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• (1A,2A,5A)-6,6-DIMETHYLBICYCLO[3.1.1]HEPTANE-2-CARBALDEHYDECAS

  Cas No: 49751-88-4

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• (1alpha,2alpha,5alpha)-6,6-Dimethylbicyclo(3.1.1)heptane-2-carbaldehyde

  Cas No: 49751-88-4

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49751-88-4 Usage

General Description

The chemical "(1alpha,2alpha,5alpha)-6,6-dimethylbicyclo[3.1.1]heptane-2-carbaldehyde" is a bicyclic compound with a carbaldehyde functional group. It has a three-dimensional structure due to the presence of a six-membered ring and a bridgehead carbon. The compound is characterized by its bicyclo[3.1.1]heptane core, with two methyl groups at positions 6 and 6, and an aldehyde group attached to position 2. It is used in the synthesis of organic compounds and pharmaceuticals as a building block, and it may also have potential applications in fragrance and flavor industries.

Check Digit Verification of cas no

The CAS Registry Mumber 49751-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,5 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 49751-88:
(7*4)+(6*9)+(5*7)+(4*5)+(3*1)+(2*8)+(1*8)=164
164 % 10 = 4
So 49751-88-4 is a valid CAS Registry Number.

InChI:InChI=1/C10H16O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h6-9H,3-5H2,1-2H3/t7-,8-,9-/m0/s1

49751-88-4Upstream product

• 132203-71-5 6,6-dimethylbicyclo[3.1.1]heptane-2-methanol 
• 56246-58-3 β-pinene oxide 
• 473-01-8 cis-myrtanol 
• 18680-26-7 pinane-2β,10-diol 
• 6712-78-3 myrtenol 
• 473-01-8 trans-myrtanol 
• 473-01-8 ((1S*,2R*,5S*)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl)methanol 

49751-88-4Downstream Products

49751-88-4Relevant articles and documents

Photocaged Hydrocarbons, Aldehydes, Ketones, Enones, and Carboxylic Acids and Esters that Release by the Norrish II Cleavage Protocol and Beyond: Controlled Photoinduced Fragrance Release

Griesbeck, Axel G.,Porschen, Bj?rn,Kropf, Christian,Landes, Agnieszka,Hinze, Olga,Huchel, Ursula,Gerke, Thomas

, p. 539 - 553 (2017/01/25)

Five families of caged fragrance compounds that allow the storage and release of the following small volatile organic molecules are described: terpene hydrocarbons, aldehydes, ketones, Michael-type α,β-unsaturated enones, and carboxylic acids and esters. These caged molecules are released by photoexcitation via carbonyl-directed hydrogen-transfer processes and subsequent C-C bond cleavage (Norrish Type II) or by didenitrogenation of diazirines.

Convenient preparation of carbonyl compounds from 1,2-diols utilizing Mitsunobu conditions

Barrero, Alejandro F.,Alvarez-Manzaneda, Enrique J.,Chahboun

, p. 1959 - 1962 (2007/10/03)

1,1-Disubstituted 1,2-diols are efficiently converted into carbonyl compounds by reaction with triphenylphosphine and diethyl azodicarboxylate. (C) 2000 Elsevier Science Ltd.

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