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CAS

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29172-41-6

Cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, acetate, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29172-41-6 Structure

  • Basic information

    1. Product Name: Cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, acetate, trans-
    2. Synonyms:
    3. CAS NO:29172-41-6
    4. Molecular Formula: C12H20O2
    5. Molecular Weight: 196.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29172-41-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, acetate, trans-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, acetate, trans-(29172-41-6)
    11. EPA Substance Registry System: Cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, acetate, trans-(29172-41-6)

  • 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: 29172-41-6(Hazardous Substances Data)

29172-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29172-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29172-41:
(7*2)+(6*9)+(5*1)+(4*7)+(3*2)+(2*4)+(1*1)=116
116 % 10 = 6
So 29172-41-6 is a valid CAS Registry Number.

29172-41-6Downstream Products

29172-41-6Relevant articles and documents

From Δ3-carene to the most biologically active insecticides: A convenient and efficient synthesis of (+)-(1R)-cis-chrysanthemic acid

Dhillon, Ranjit S,Gautam, Veena K,Singh, Swaranjit,Singh, Jasvinder

, p. 574 - 578 (2007/10/02)

A convenient and economical synthesis of (+)-(1R)-cis-chrysanthemic acid from Δ3-carene is reported.

Synthesis of 3-Phenoxybenzyl 1R-cis-2,2-Dimethyl-3-(acyloxy or alkoxymethyl)cyclopropanecarboxylate from (+)-3-Carene

Bhosale, S. S.,Mahamulkar, B. G.,Gore, K. G.,Kulkarni, G. H.,Mitra, R. B.

, p. 216 - 219 (2007/10/02)

The synthesis of 3-phenoxybenzyl 1R-cis-2,2-dimethyl-3-acetoxymethylcyclopropanecarboxylate (VI) and 3-phenoxybenzyl 1R-cis-2,2-dimethyl-3-ethoxymethylcyclopropanecarboxylate (VII) has been described from a common intermediate, viz.2,2-dimethyl-3-(2,2-eth

Synthesis of Methyl 1R(+)-cis-Chrysanthemate and Methyl 1S(+)-cis-2,2-Dimethyl-3-(2-phenylprop-1-enyl)cyclopropane-1-carboxylate from (+)-Car-3-ene

Bhat, N. G.,Mane, B. M.,Kulkarni, G. H.,Mitra, R. B.

, p. 204 - 206 (2007/10/02)

Synthesis of (+)-dihydrochrysanthemolactone (III), methyl 1R(+)-cis-chrysanthemate (II) and methyl 1S(+)-cis-2,2-dimethyl-3-(2-phenylprop-1-enyl)cyclopropane-1-carboxylate (XIII) has been achieved from a common intermediate 2,2-dimethyl-3-(2-methyl-2-hydroxypropyl)-cis-1-acetonylcyclopropane (IV), which is obtainable from (+)-car-3-ene by a known procedure.

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